← Back to variant description
GeneBe API Showcase
This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.
API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.
Documentation & Advanced Usage
• Complete API documentation:docs.genebe.net/docs/api/overview/
• Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/
• Python client for pandas:pypi.org/project/genebe/
• Java CLI for VCF files:github.com/pstawinski/genebe-cli
• All tools documented at:docs.genebe.net
API Request Examples for Variant: 18-37253912-T-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=18&pos=37253912&ref=T&alt=A&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 4,
"criteria": [
"BS2"
],
"effects": [
"missense_variant"
],
"gene_symbol": "CELF4",
"hgnc_id": 14015,
"hgvs_c": "c.1439A>T",
"hgvs_p": "p.Gln480Leu",
"inheritance_mode": "AD",
"pathogenic_score": 0,
"score": -4,
"transcript": "NM_001353740.2",
"verdict": "Likely_benign"
}
],
"acmg_classification": "Likely_benign",
"acmg_criteria": "BS2",
"acmg_score": -4,
"allele_count_reference_population": 6,
"alphamissense_prediction": null,
"alphamissense_score": 0.473,
"alt": "A",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Uncertain_significance",
"bayesdelnoaf_score": -0.04,
"chr": "18",
"clinvar_classification": "",
"clinvar_disease": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"computational_prediction_selected": "Uncertain_significance",
"computational_score_selected": 0.5933456420898438,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 486,
"aa_ref": "S",
"aa_start": 454,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3820,
"cdna_start": 1517,
"cds_end": null,
"cds_length": 1461,
"cds_start": 1360,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_020180.4",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1360A>T",
"hgvs_p": "p.Ser454Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000420428.7",
"protein_coding": true,
"protein_id": "NP_064565.1",
"strand": false,
"transcript": "NM_020180.4",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 486,
"aa_ref": "S",
"aa_start": 454,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 3820,
"cdna_start": 1517,
"cds_end": null,
"cds_length": 1461,
"cds_start": 1360,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000420428.7",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1360A>T",
"hgvs_p": "p.Ser454Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_020180.4",
"protein_coding": true,
"protein_id": "ENSP00000410584.2",
"strand": false,
"transcript": "ENST00000420428.7",
"transcript_support_level": 5
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 486,
"aa_ref": "S",
"aa_start": 454,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1461,
"cdna_start": 1360,
"cds_end": null,
"cds_length": 1461,
"cds_start": 1360,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000591282.5",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1360A>T",
"hgvs_p": "p.Ser454Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000464794.1",
"strand": false,
"transcript": "ENST00000591282.5",
"transcript_support_level": 1
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 485,
"aa_ref": "S",
"aa_start": 453,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 1906,
"cdna_start": 1543,
"cds_end": null,
"cds_length": 1458,
"cds_start": 1357,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000603232.6",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1357A>T",
"hgvs_p": "p.Ser453Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000474788.2",
"strand": false,
"transcript": "ENST00000603232.6",
"transcript_support_level": 1
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 484,
"aa_ref": "S",
"aa_start": 452,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 1853,
"cdna_start": 1478,
"cds_end": null,
"cds_length": 1455,
"cds_start": 1354,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000361795.9",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1354A>T",
"hgvs_p": "p.Ser452Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000355089.4",
"strand": false,
"transcript": "ENST00000361795.9",
"transcript_support_level": 2
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 484,
"aa_ref": "S",
"aa_start": 452,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3757,
"cdna_start": 1461,
"cds_end": null,
"cds_length": 1455,
"cds_start": 1354,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000591287.5",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1354A>T",
"hgvs_p": "p.Ser452Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000464917.1",
"strand": false,
"transcript": "ENST00000591287.5",
"transcript_support_level": 1
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 448,
"aa_ref": "S",
"aa_start": 416,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3542,
"cdna_start": 1246,
"cds_end": null,
"cds_length": 1347,
"cds_start": 1246,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "ENST00000334919.9",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1246A>T",
"hgvs_p": "p.Ser416Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000335631.4",
"strand": false,
"transcript": "ENST00000334919.9",
"transcript_support_level": 1
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 545,
"aa_ref": "Q",
"aa_start": 480,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3984,
"cdna_start": 1596,
"cds_end": null,
"cds_length": 1638,
"cds_start": 1439,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "NM_001353740.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1439A>T",
"hgvs_p": "p.Gln480Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340669.1",
"strand": false,
"transcript": "NM_001353740.2",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 544,
"aa_ref": "Q",
"aa_start": 479,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3981,
"cdna_start": 1593,
"cds_end": null,
"cds_length": 1635,
"cds_start": 1436,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "NM_001353749.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1436A>T",
"hgvs_p": "p.Gln479Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340678.1",
"strand": false,
"transcript": "NM_001353749.2",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 536,
"aa_ref": "Q",
"aa_start": 480,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3899,
"cdna_start": 1596,
"cds_end": null,
"cds_length": 1611,
"cds_start": 1439,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "NM_001353734.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1439A>T",
"hgvs_p": "p.Gln480Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340663.1",
"strand": false,
"transcript": "NM_001353734.2",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 535,
"aa_ref": "Q",
"aa_start": 479,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3896,
"cdna_start": 1593,
"cds_end": null,
"cds_length": 1608,
"cds_start": 1436,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "NM_001353731.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1436A>T",
"hgvs_p": "p.Gln479Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340660.1",
"strand": false,
"transcript": "NM_001353731.2",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 535,
"aa_ref": "Q",
"aa_start": 479,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3896,
"cdna_start": 1593,
"cds_end": null,
"cds_length": 1608,
"cds_start": 1436,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "NM_001353746.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1436A>T",
"hgvs_p": "p.Gln479Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340675.1",
"strand": false,
"transcript": "NM_001353746.2",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 534,
"aa_ref": "Q",
"aa_start": 469,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3951,
"cdna_start": 1563,
"cds_end": null,
"cds_length": 1605,
"cds_start": 1406,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "NM_001353735.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1406A>T",
"hgvs_p": "p.Gln469Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340664.1",
"strand": false,
"transcript": "NM_001353735.2",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 531,
"aa_ref": "Q",
"aa_start": 466,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3942,
"cdna_start": 1554,
"cds_end": null,
"cds_length": 1596,
"cds_start": 1397,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "NM_001353733.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1397A>T",
"hgvs_p": "p.Gln466Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340662.1",
"strand": false,
"transcript": "NM_001353733.2",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 526,
"aa_ref": "Q",
"aa_start": 470,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3869,
"cdna_start": 1566,
"cds_end": null,
"cds_length": 1581,
"cds_start": 1409,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "NM_001353703.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1409A>T",
"hgvs_p": "p.Gln470Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340632.1",
"strand": false,
"transcript": "NM_001353703.2",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 525,
"aa_ref": "Q",
"aa_start": 469,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3866,
"cdna_start": 1563,
"cds_end": null,
"cds_length": 1578,
"cds_start": 1406,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "NM_001353726.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1406A>T",
"hgvs_p": "p.Gln469Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340655.1",
"strand": false,
"transcript": "NM_001353726.2",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 525,
"aa_ref": "Q",
"aa_start": 469,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3866,
"cdna_start": 1563,
"cds_end": null,
"cds_length": 1578,
"cds_start": 1406,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "NM_001353741.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1406A>T",
"hgvs_p": "p.Gln469Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340670.1",
"strand": false,
"transcript": "NM_001353741.2",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 524,
"aa_ref": "Q",
"aa_start": 468,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3863,
"cdna_start": 1560,
"cds_end": null,
"cds_length": 1575,
"cds_start": 1403,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "NM_001353728.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1403A>T",
"hgvs_p": "p.Gln468Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340657.1",
"strand": false,
"transcript": "NM_001353728.2",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 523,
"aa_ref": "Q",
"aa_start": 467,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3860,
"cdna_start": 1557,
"cds_end": null,
"cds_length": 1572,
"cds_start": 1400,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "NM_001353739.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1400A>T",
"hgvs_p": "p.Gln467Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340668.1",
"strand": false,
"transcript": "NM_001353739.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 505,
"aa_ref": "S",
"aa_start": 473,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2291,
"cdna_start": 1516,
"cds_end": null,
"cds_length": 1518,
"cds_start": 1417,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000899364.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1417A>T",
"hgvs_p": "p.Ser473Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000569423.1",
"strand": false,
"transcript": "ENST00000899364.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 504,
"aa_ref": "S",
"aa_start": 472,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3874,
"cdna_start": 1571,
"cds_end": null,
"cds_length": 1515,
"cds_start": 1414,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353742.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1414A>T",
"hgvs_p": "p.Ser472Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340671.1",
"strand": false,
"transcript": "NM_001353742.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 504,
"aa_ref": "S",
"aa_start": 472,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2404,
"cdna_start": 1611,
"cds_end": null,
"cds_length": 1515,
"cds_start": 1414,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000899359.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1414A>T",
"hgvs_p": "p.Ser472Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000569418.1",
"strand": false,
"transcript": "ENST00000899359.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 502,
"aa_ref": "S",
"aa_start": 470,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3699,
"cdna_start": 1564,
"cds_end": null,
"cds_length": 1509,
"cds_start": 1408,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000970539.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1408A>T",
"hgvs_p": "p.Ser470Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000640598.1",
"strand": false,
"transcript": "ENST00000970539.1",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 498,
"aa_ref": "Q",
"aa_start": 442,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3785,
"cdna_start": 1482,
"cds_end": null,
"cds_length": 1497,
"cds_start": 1325,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353715.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1325A>T",
"hgvs_p": "p.Gln442Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340644.1",
"strand": false,
"transcript": "NM_001353715.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 496,
"aa_ref": "S",
"aa_start": 464,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3850,
"cdna_start": 1547,
"cds_end": null,
"cds_length": 1491,
"cds_start": 1390,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353717.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1390A>T",
"hgvs_p": "p.Ser464Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340646.1",
"strand": false,
"transcript": "NM_001353717.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 495,
"aa_ref": "S",
"aa_start": 463,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3847,
"cdna_start": 1544,
"cds_end": null,
"cds_length": 1488,
"cds_start": 1387,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353707.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1387A>T",
"hgvs_p": "p.Ser463Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340636.1",
"strand": false,
"transcript": "NM_001353707.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 493,
"aa_ref": "S",
"aa_start": 461,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3841,
"cdna_start": 1538,
"cds_end": null,
"cds_length": 1482,
"cds_start": 1381,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353705.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1381A>T",
"hgvs_p": "p.Ser461Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340634.1",
"strand": false,
"transcript": "NM_001353705.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 485,
"aa_ref": "S",
"aa_start": 453,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3817,
"cdna_start": 1514,
"cds_end": null,
"cds_length": 1458,
"cds_start": 1357,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001025087.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1357A>T",
"hgvs_p": "p.Ser453Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001020258.1",
"strand": false,
"transcript": "NM_001025087.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 485,
"aa_ref": "S",
"aa_start": 453,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3817,
"cdna_start": 1514,
"cds_end": null,
"cds_length": 1458,
"cds_start": 1357,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353698.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1357A>T",
"hgvs_p": "p.Ser453Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340627.1",
"strand": false,
"transcript": "NM_001353698.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 485,
"aa_ref": "S",
"aa_start": 453,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3817,
"cdna_start": 1514,
"cds_end": null,
"cds_length": 1458,
"cds_start": 1357,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353744.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1357A>T",
"hgvs_p": "p.Ser453Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340673.1",
"strand": false,
"transcript": "NM_001353744.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 485,
"aa_ref": "S",
"aa_start": 453,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3817,
"cdna_start": 1514,
"cds_end": null,
"cds_length": 1458,
"cds_start": 1357,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353751.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1357A>T",
"hgvs_p": "p.Ser453Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340680.1",
"strand": false,
"transcript": "NM_001353751.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 485,
"aa_ref": "S",
"aa_start": 453,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2599,
"cdna_start": 1619,
"cds_end": null,
"cds_length": 1458,
"cds_start": 1357,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000899355.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1357A>T",
"hgvs_p": "p.Ser453Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000569414.1",
"strand": false,
"transcript": "ENST00000899355.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 485,
"aa_ref": "S",
"aa_start": 453,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2306,
"cdna_start": 1520,
"cds_end": null,
"cds_length": 1458,
"cds_start": 1357,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000899361.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1357A>T",
"hgvs_p": "p.Ser453Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000569420.1",
"strand": false,
"transcript": "ENST00000899361.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 484,
"aa_ref": "S",
"aa_start": 452,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3814,
"cdna_start": 1511,
"cds_end": null,
"cds_length": 1455,
"cds_start": 1354,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001025088.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1354A>T",
"hgvs_p": "p.Ser452Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001020259.1",
"strand": false,
"transcript": "NM_001025088.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 484,
"aa_ref": "S",
"aa_start": 452,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3814,
"cdna_start": 1511,
"cds_end": null,
"cds_length": 1455,
"cds_start": 1354,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001330603.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1354A>T",
"hgvs_p": "p.Ser452Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001317532.1",
"strand": false,
"transcript": "NM_001330603.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 484,
"aa_ref": "S",
"aa_start": 452,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3814,
"cdna_start": 1511,
"cds_end": null,
"cds_length": 1455,
"cds_start": 1354,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353724.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1354A>T",
"hgvs_p": "p.Ser452Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340653.1",
"strand": false,
"transcript": "NM_001353724.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 484,
"aa_ref": "S",
"aa_start": 452,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3814,
"cdna_start": 1511,
"cds_end": null,
"cds_length": 1455,
"cds_start": 1354,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353738.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1354A>T",
"hgvs_p": "p.Ser452Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340667.1",
"strand": false,
"transcript": "NM_001353738.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 484,
"aa_ref": "S",
"aa_start": 452,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3814,
"cdna_start": 1511,
"cds_end": null,
"cds_length": 1455,
"cds_start": 1354,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353745.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1354A>T",
"hgvs_p": "p.Ser452Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340674.1",
"strand": false,
"transcript": "NM_001353745.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 484,
"aa_ref": "S",
"aa_start": 452,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1836,
"cdna_start": 1461,
"cds_end": null,
"cds_length": 1455,
"cds_start": 1354,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000601019.5",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1354A>T",
"hgvs_p": "p.Ser452Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000469627.1",
"strand": false,
"transcript": "ENST00000601019.5",
"transcript_support_level": 5
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 484,
"aa_ref": "S",
"aa_start": 452,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2330,
"cdna_start": 1533,
"cds_end": null,
"cds_length": 1455,
"cds_start": 1354,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000899360.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1354A>T",
"hgvs_p": "p.Ser452Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000569419.1",
"strand": false,
"transcript": "ENST00000899360.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 483,
"aa_ref": "S",
"aa_start": 451,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3811,
"cdna_start": 1508,
"cds_end": null,
"cds_length": 1452,
"cds_start": 1351,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353702.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1351A>T",
"hgvs_p": "p.Ser451Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340631.1",
"strand": false,
"transcript": "NM_001353702.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 483,
"aa_ref": "S",
"aa_start": 451,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3811,
"cdna_start": 1508,
"cds_end": null,
"cds_length": 1452,
"cds_start": 1351,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353718.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1351A>T",
"hgvs_p": "p.Ser451Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340647.1",
"strand": false,
"transcript": "NM_001353718.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 483,
"aa_ref": "S",
"aa_start": 451,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2299,
"cdna_start": 1506,
"cds_end": null,
"cds_length": 1452,
"cds_start": 1351,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000899362.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1351A>T",
"hgvs_p": "p.Ser451Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000569421.1",
"strand": false,
"transcript": "ENST00000899362.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 482,
"aa_ref": "S",
"aa_start": 450,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3808,
"cdna_start": 1505,
"cds_end": null,
"cds_length": 1449,
"cds_start": 1348,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353712.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1348A>T",
"hgvs_p": "p.Ser450Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340641.1",
"strand": false,
"transcript": "NM_001353712.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 477,
"aa_ref": "S",
"aa_start": 445,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2561,
"cdna_start": 1400,
"cds_end": null,
"cds_length": 1434,
"cds_start": 1333,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000970542.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1333A>T",
"hgvs_p": "p.Ser445Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000640601.1",
"strand": false,
"transcript": "ENST00000970542.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 475,
"aa_ref": "S",
"aa_start": 443,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3787,
"cdna_start": 1484,
"cds_end": null,
"cds_length": 1428,
"cds_start": 1327,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353709.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1327A>T",
"hgvs_p": "p.Ser443Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340638.1",
"strand": false,
"transcript": "NM_001353709.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 475,
"aa_ref": "S",
"aa_start": 443,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3787,
"cdna_start": 1484,
"cds_end": null,
"cds_length": 1428,
"cds_start": 1327,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353748.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1327A>T",
"hgvs_p": "p.Ser443Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340677.1",
"strand": false,
"transcript": "NM_001353748.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 475,
"aa_ref": "S",
"aa_start": 443,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3787,
"cdna_start": 1484,
"cds_end": null,
"cds_length": 1428,
"cds_start": 1327,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353752.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1327A>T",
"hgvs_p": "p.Ser443Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340681.1",
"strand": false,
"transcript": "NM_001353752.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 475,
"aa_ref": "S",
"aa_start": 443,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2405,
"cdna_start": 1618,
"cds_end": null,
"cds_length": 1428,
"cds_start": 1327,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000899357.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1327A>T",
"hgvs_p": "p.Ser443Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000569416.1",
"strand": false,
"transcript": "ENST00000899357.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 475,
"aa_ref": "S",
"aa_start": 443,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3789,
"cdna_start": 1498,
"cds_end": null,
"cds_length": 1428,
"cds_start": 1327,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000970536.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1327A>T",
"hgvs_p": "p.Ser443Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000640595.1",
"strand": false,
"transcript": "ENST00000970536.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 474,
"aa_ref": "S",
"aa_start": 442,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3784,
"cdna_start": 1481,
"cds_end": null,
"cds_length": 1425,
"cds_start": 1324,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353695.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1324A>T",
"hgvs_p": "p.Ser442Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340624.1",
"strand": false,
"transcript": "NM_001353695.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 474,
"aa_ref": "S",
"aa_start": 442,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3784,
"cdna_start": 1481,
"cds_end": null,
"cds_length": 1425,
"cds_start": 1324,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353710.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1324A>T",
"hgvs_p": "p.Ser442Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340639.1",
"strand": false,
"transcript": "NM_001353710.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 474,
"aa_ref": "S",
"aa_start": 442,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3784,
"cdna_start": 1481,
"cds_end": null,
"cds_length": 1425,
"cds_start": 1324,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353721.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1324A>T",
"hgvs_p": "p.Ser442Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340650.1",
"strand": false,
"transcript": "NM_001353721.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 474,
"aa_ref": "S",
"aa_start": 442,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3784,
"cdna_start": 1481,
"cds_end": null,
"cds_length": 1425,
"cds_start": 1324,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353750.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1324A>T",
"hgvs_p": "p.Ser442Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340679.1",
"strand": false,
"transcript": "NM_001353750.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 474,
"aa_ref": "S",
"aa_start": 442,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3784,
"cdna_start": 1481,
"cds_end": null,
"cds_length": 1425,
"cds_start": 1324,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353753.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1324A>T",
"hgvs_p": "p.Ser442Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340682.1",
"strand": false,
"transcript": "NM_001353753.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 474,
"aa_ref": "S",
"aa_start": 442,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3784,
"cdna_start": 1481,
"cds_end": null,
"cds_length": 1425,
"cds_start": 1324,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353755.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1324A>T",
"hgvs_p": "p.Ser442Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340684.1",
"strand": false,
"transcript": "NM_001353755.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 474,
"aa_ref": "S",
"aa_start": 442,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2368,
"cdna_start": 1582,
"cds_end": null,
"cds_length": 1425,
"cds_start": 1324,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000899358.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1324A>T",
"hgvs_p": "p.Ser442Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000569417.1",
"strand": false,
"transcript": "ENST00000899358.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 473,
"aa_ref": "S",
"aa_start": 441,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3781,
"cdna_start": 1478,
"cds_end": null,
"cds_length": 1422,
"cds_start": 1321,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353711.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1321A>T",
"hgvs_p": "p.Ser441Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340640.1",
"strand": false,
"transcript": "NM_001353711.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 473,
"aa_ref": "S",
"aa_start": 441,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3781,
"cdna_start": 1478,
"cds_end": null,
"cds_length": 1422,
"cds_start": 1321,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353714.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1321A>T",
"hgvs_p": "p.Ser441Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340643.1",
"strand": false,
"transcript": "NM_001353714.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 473,
"aa_ref": "S",
"aa_start": 441,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3781,
"cdna_start": 1478,
"cds_end": null,
"cds_length": 1422,
"cds_start": 1321,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353725.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1321A>T",
"hgvs_p": "p.Ser441Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340654.1",
"strand": false,
"transcript": "NM_001353725.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 473,
"aa_ref": "S",
"aa_start": 441,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2467,
"cdna_start": 1674,
"cds_end": null,
"cds_length": 1422,
"cds_start": 1321,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "ENST00000899356.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1321A>T",
"hgvs_p": "p.Ser441Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000569415.1",
"strand": false,
"transcript": "ENST00000899356.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 458,
"aa_ref": "S",
"aa_start": 426,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3736,
"cdna_start": 1433,
"cds_end": null,
"cds_length": 1377,
"cds_start": 1276,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353708.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1276A>T",
"hgvs_p": "p.Ser426Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340637.1",
"strand": false,
"transcript": "NM_001353708.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 457,
"aa_ref": "S",
"aa_start": 425,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3733,
"cdna_start": 1430,
"cds_end": null,
"cds_length": 1374,
"cds_start": 1273,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353696.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1273A>T",
"hgvs_p": "p.Ser425Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340625.1",
"strand": false,
"transcript": "NM_001353696.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 457,
"aa_ref": "S",
"aa_start": 425,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3733,
"cdna_start": 1430,
"cds_end": null,
"cds_length": 1374,
"cds_start": 1273,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353723.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1273A>T",
"hgvs_p": "p.Ser425Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340652.1",
"strand": false,
"transcript": "NM_001353723.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 457,
"aa_ref": "S",
"aa_start": 425,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3733,
"cdna_start": 1430,
"cds_end": null,
"cds_length": 1374,
"cds_start": 1273,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353743.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1273A>T",
"hgvs_p": "p.Ser425Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340672.1",
"strand": false,
"transcript": "NM_001353743.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 457,
"aa_ref": "S",
"aa_start": 425,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2197,
"cdna_start": 1468,
"cds_end": null,
"cds_length": 1374,
"cds_start": 1273,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "ENST00000970544.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1273A>T",
"hgvs_p": "p.Ser425Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000640603.1",
"strand": false,
"transcript": "ENST00000970544.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 456,
"aa_ref": "S",
"aa_start": 424,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3730,
"cdna_start": 1427,
"cds_end": null,
"cds_length": 1371,
"cds_start": 1270,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353729.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1270A>T",
"hgvs_p": "p.Ser424Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340658.1",
"strand": false,
"transcript": "NM_001353729.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 456,
"aa_ref": "S",
"aa_start": 424,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3730,
"cdna_start": 1427,
"cds_end": null,
"cds_length": 1371,
"cds_start": 1270,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353730.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1270A>T",
"hgvs_p": "p.Ser424Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340659.1",
"strand": false,
"transcript": "NM_001353730.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 456,
"aa_ref": "S",
"aa_start": 424,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3730,
"cdna_start": 1427,
"cds_end": null,
"cds_length": 1371,
"cds_start": 1270,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353736.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1270A>T",
"hgvs_p": "p.Ser424Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340665.1",
"strand": false,
"transcript": "NM_001353736.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 456,
"aa_ref": "S",
"aa_start": 424,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3730,
"cdna_start": 1427,
"cds_end": null,
"cds_length": 1371,
"cds_start": 1270,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353747.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1270A>T",
"hgvs_p": "p.Ser424Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340676.1",
"strand": false,
"transcript": "NM_001353747.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 456,
"aa_ref": "S",
"aa_start": 424,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3730,
"cdna_start": 1427,
"cds_end": null,
"cds_length": 1371,
"cds_start": 1270,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353754.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1270A>T",
"hgvs_p": "p.Ser424Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340683.1",
"strand": false,
"transcript": "NM_001353754.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 456,
"aa_ref": "S",
"aa_start": 424,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3622,
"cdna_start": 1487,
"cds_end": null,
"cds_length": 1371,
"cds_start": 1270,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "ENST00000970538.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1270A>T",
"hgvs_p": "p.Ser424Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000640597.1",
"strand": false,
"transcript": "ENST00000970538.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 455,
"aa_ref": "S",
"aa_start": 423,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3727,
"cdna_start": 1424,
"cds_end": null,
"cds_length": 1368,
"cds_start": 1267,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353716.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1267A>T",
"hgvs_p": "p.Ser423Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340645.1",
"strand": false,
"transcript": "NM_001353716.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 455,
"aa_ref": "S",
"aa_start": 423,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3727,
"cdna_start": 1424,
"cds_end": null,
"cds_length": 1368,
"cds_start": 1267,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353737.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1267A>T",
"hgvs_p": "p.Ser423Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340666.1",
"strand": false,
"transcript": "NM_001353737.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 455,
"aa_ref": "S",
"aa_start": 423,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3715,
"cdna_start": 1419,
"cds_end": null,
"cds_length": 1368,
"cds_start": 1267,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "ENST00000970537.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1267A>T",
"hgvs_p": "p.Ser423Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000640596.1",
"strand": false,
"transcript": "ENST00000970537.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 448,
"aa_ref": "S",
"aa_start": 416,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3706,
"cdna_start": 1403,
"cds_end": null,
"cds_length": 1347,
"cds_start": 1246,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001025089.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1246A>T",
"hgvs_p": "p.Ser416Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001020260.1",
"strand": false,
"transcript": "NM_001025089.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 447,
"aa_ref": "S",
"aa_start": 415,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3703,
"cdna_start": 1400,
"cds_end": null,
"cds_length": 1344,
"cds_start": 1243,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353697.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1243A>T",
"hgvs_p": "p.Ser415Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340626.1",
"strand": false,
"transcript": "NM_001353697.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 447,
"aa_ref": "S",
"aa_start": 415,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3703,
"cdna_start": 1400,
"cds_end": null,
"cds_length": 1344,
"cds_start": 1243,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353700.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1243A>T",
"hgvs_p": "p.Ser415Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340629.1",
"strand": false,
"transcript": "NM_001353700.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 447,
"aa_ref": "S",
"aa_start": 415,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3703,
"cdna_start": 1400,
"cds_end": null,
"cds_length": 1344,
"cds_start": 1243,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353713.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1243A>T",
"hgvs_p": "p.Ser415Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340642.1",
"strand": false,
"transcript": "NM_001353713.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 447,
"aa_ref": "S",
"aa_start": 415,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3703,
"cdna_start": 1400,
"cds_end": null,
"cds_length": 1344,
"cds_start": 1243,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353719.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1243A>T",
"hgvs_p": "p.Ser415Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340648.1",
"strand": false,
"transcript": "NM_001353719.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 446,
"aa_ref": "S",
"aa_start": 414,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3700,
"cdna_start": 1397,
"cds_end": null,
"cds_length": 1341,
"cds_start": 1240,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353699.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1240A>T",
"hgvs_p": "p.Ser414Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340628.1",
"strand": false,
"transcript": "NM_001353699.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 446,
"aa_ref": "S",
"aa_start": 414,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3700,
"cdna_start": 1397,
"cds_end": null,
"cds_length": 1341,
"cds_start": 1240,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353706.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1240A>T",
"hgvs_p": "p.Ser414Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340635.1",
"strand": false,
"transcript": "NM_001353706.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 446,
"aa_ref": "S",
"aa_start": 414,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3700,
"cdna_start": 1397,
"cds_end": null,
"cds_length": 1341,
"cds_start": 1240,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353720.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1240A>T",
"hgvs_p": "p.Ser414Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340649.1",
"strand": false,
"transcript": "NM_001353720.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 446,
"aa_ref": "S",
"aa_start": 414,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3700,
"cdna_start": 1397,
"cds_end": null,
"cds_length": 1341,
"cds_start": 1240,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353727.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1240A>T",
"hgvs_p": "p.Ser414Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340656.1",
"strand": false,
"transcript": "NM_001353727.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 446,
"aa_ref": "S",
"aa_start": 414,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3700,
"cdna_start": 1397,
"cds_end": null,
"cds_length": 1341,
"cds_start": 1240,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353732.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1240A>T",
"hgvs_p": "p.Ser414Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340661.1",
"strand": false,
"transcript": "NM_001353732.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 445,
"aa_ref": "S",
"aa_start": 413,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3697,
"cdna_start": 1394,
"cds_end": null,
"cds_length": 1338,
"cds_start": 1237,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353722.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1237A>T",
"hgvs_p": "p.Ser413Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340651.1",
"strand": false,
"transcript": "NM_001353722.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 445,
"aa_ref": "S",
"aa_start": 413,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2164,
"cdna_start": 1405,
"cds_end": null,
"cds_length": 1338,
"cds_start": 1237,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "ENST00000899363.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1237A>T",
"hgvs_p": "p.Ser413Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000569422.1",
"strand": false,
"transcript": "ENST00000899363.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 435,
"aa_ref": "S",
"aa_start": 403,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1733,
"cdna_start": 1342,
"cds_end": null,
"cds_length": 1308,
"cds_start": 1207,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "ENST00000899365.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1207A>T",
"hgvs_p": "p.Ser403Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000569424.1",
"strand": false,
"transcript": "ENST00000899365.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 430,
"aa_ref": "S",
"aa_start": 398,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1628,
"cdna_start": 1269,
"cds_end": null,
"cds_length": 1293,
"cds_start": 1192,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "ENST00000970546.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1192A>T",
"hgvs_p": "p.Ser398Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000640605.1",
"strand": false,
"transcript": "ENST00000970546.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 408,
"aa_ref": "S",
"aa_start": 376,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2455,
"cdna_start": 1294,
"cds_end": null,
"cds_length": 1227,
"cds_start": 1126,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000970541.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1126A>T",
"hgvs_p": "p.Ser376Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000640600.1",
"strand": false,
"transcript": "ENST00000970541.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 397,
"aa_ref": "S",
"aa_start": 365,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2424,
"cdna_start": 1268,
"cds_end": null,
"cds_length": 1194,
"cds_start": 1093,
"consequences": [
"missense_variant"
],
"exon_count": 10,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000970540.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1093A>T",
"hgvs_p": "p.Ser365Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000640599.1",
"strand": false,
"transcript": "ENST00000970540.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 395,
"aa_ref": "S",
"aa_start": 363,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3489,
"cdna_start": 1186,
"cds_end": null,
"cds_length": 1188,
"cds_start": 1087,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "ENST00000931906.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1087A>T",
"hgvs_p": "p.Ser363Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000601965.1",
"strand": false,
"transcript": "ENST00000931906.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 362,
"aa_ref": "S",
"aa_start": 330,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3441,
"cdna_start": 1138,
"cds_end": null,
"cds_length": 1089,
"cds_start": 988,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353756.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.988A>T",
"hgvs_p": "p.Ser330Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340685.1",
"strand": false,
"transcript": "NM_001353756.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 361,
"aa_ref": "S",
"aa_start": 329,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3438,
"cdna_start": 1135,
"cds_end": null,
"cds_length": 1086,
"cds_start": 985,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353761.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.985A>T",
"hgvs_p": "p.Ser329Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340690.1",
"strand": false,
"transcript": "NM_001353761.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 358,
"aa_ref": "S",
"aa_start": 326,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1547,
"cdna_start": 1187,
"cds_end": null,
"cds_length": 1077,
"cds_start": 976,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000970545.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.976A>T",
"hgvs_p": "p.Ser326Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000640604.1",
"strand": false,
"transcript": "ENST00000970545.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 353,
"aa_ref": "S",
"aa_start": 321,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3414,
"cdna_start": 1111,
"cds_end": null,
"cds_length": 1062,
"cds_start": 961,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353757.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.961A>T",
"hgvs_p": "p.Ser321Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340686.1",
"strand": false,
"transcript": "NM_001353757.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 352,
"aa_ref": "S",
"aa_start": 320,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3411,
"cdna_start": 1108,
"cds_end": null,
"cds_length": 1059,
"cds_start": 958,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353759.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.958A>T",
"hgvs_p": "p.Ser320Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340688.1",
"strand": false,
"transcript": "NM_001353759.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 352,
"aa_ref": "S",
"aa_start": 320,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3411,
"cdna_start": 1108,
"cds_end": null,
"cds_length": 1059,
"cds_start": 958,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NM_001353760.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.958A>T",
"hgvs_p": "p.Ser320Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340689.1",
"strand": false,
"transcript": "NM_001353760.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 324,
"aa_ref": "S",
"aa_start": 292,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3327,
"cdna_start": 1024,
"cds_end": null,
"cds_length": 975,
"cds_start": 874,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NM_001353758.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.874A>T",
"hgvs_p": "p.Ser292Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001340687.1",
"strand": false,
"transcript": "NM_001353758.2",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 309,
"aa_ref": "S",
"aa_start": 277,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2002,
"cdna_start": 846,
"cds_end": null,
"cds_length": 930,
"cds_start": 829,
"consequences": [
"missense_variant"
],
"exon_count": 9,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000970543.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.829A>T",
"hgvs_p": "p.Ser277Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000640602.1",
"strand": false,
"transcript": "ENST00000970543.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 180,
"aa_ref": "S",
"aa_start": 163,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 556,
"cdna_start": 499,
"cds_end": null,
"cds_length": 544,
"cds_start": 487,
"consequences": [
"missense_variant"
],
"exon_count": 6,
"exon_rank": 6,
"exon_rank_end": null,
"feature": "ENST00000589386.5",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.487A>T",
"hgvs_p": "p.Ser163Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000465125.2",
"strand": false,
"transcript": "ENST00000589386.5",
"transcript_support_level": 3
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 151,
"aa_ref": "S",
"aa_start": 119,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2651,
"cdna_start": 355,
"cds_end": null,
"cds_length": 456,
"cds_start": 355,
"consequences": [
"missense_variant"
],
"exon_count": 6,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000588591.5",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.355A>T",
"hgvs_p": "p.Ser119Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000468256.1",
"strand": false,
"transcript": "ENST00000588591.5",
"transcript_support_level": 3
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 137,
"aa_ref": "S",
"aa_start": 114,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 426,
"cdna_start": 352,
"cds_end": null,
"cds_length": 414,
"cds_start": 340,
"consequences": [
"missense_variant"
],
"exon_count": 5,
"exon_rank": 5,
"exon_rank_end": null,
"feature": "ENST00000593271.5",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.340A>T",
"hgvs_p": "p.Ser114Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000464996.2",
"strand": false,
"transcript": "ENST00000593271.5",
"transcript_support_level": 3
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 114,
"aa_ref": "S",
"aa_start": 82,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2542,
"cdna_start": 246,
"cds_end": null,
"cds_length": 345,
"cds_start": 244,
"consequences": [
"missense_variant"
],
"exon_count": 4,
"exon_rank": 3,
"exon_rank_end": null,
"feature": "ENST00000586009.5",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.244A>T",
"hgvs_p": "p.Ser82Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000465348.1",
"strand": false,
"transcript": "ENST00000586009.5",
"transcript_support_level": 3
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 68,
"aa_ref": "S",
"aa_start": 36,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 532,
"cdna_start": 108,
"cds_end": null,
"cds_length": 207,
"cds_start": 106,
"consequences": [
"missense_variant"
],
"exon_count": 4,
"exon_rank": 2,
"exon_rank_end": null,
"feature": "ENST00000587911.5",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.106A>T",
"hgvs_p": "p.Ser36Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000471616.1",
"strand": false,
"transcript": "ENST00000587911.5",
"transcript_support_level": 2
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 545,
"aa_ref": "Q",
"aa_start": 480,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6168,
"cdna_start": 1596,
"cds_end": null,
"cds_length": 1638,
"cds_start": 1439,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "XM_047437628.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1439A>T",
"hgvs_p": "p.Gln480Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293584.1",
"strand": false,
"transcript": "XM_047437628.1",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 544,
"aa_ref": "Q",
"aa_start": 479,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6165,
"cdna_start": 1593,
"cds_end": null,
"cds_length": 1635,
"cds_start": 1436,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "XM_047437629.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1436A>T",
"hgvs_p": "p.Gln479Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293585.1",
"strand": false,
"transcript": "XM_047437629.1",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 535,
"aa_ref": "Q",
"aa_start": 470,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6138,
"cdna_start": 1566,
"cds_end": null,
"cds_length": 1608,
"cds_start": 1409,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "XM_047437630.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1409A>T",
"hgvs_p": "p.Gln470Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293586.1",
"strand": false,
"transcript": "XM_047437630.1",
"transcript_support_level": null
},
{
"aa_alt": "L",
"aa_end": null,
"aa_length": 534,
"aa_ref": "Q",
"aa_start": 469,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6135,
"cdna_start": 1563,
"cds_end": null,
"cds_length": 1605,
"cds_start": 1406,
"consequences": [
"missense_variant"
],
"exon_count": 14,
"exon_rank": 13,
"exon_rank_end": null,
"feature": "XM_047437631.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1406A>T",
"hgvs_p": "p.Gln469Leu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293587.1",
"strand": false,
"transcript": "XM_047437631.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 506,
"aa_ref": "S",
"aa_start": 474,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6149,
"cdna_start": 1577,
"cds_end": null,
"cds_length": 1521,
"cds_start": 1420,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437632.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1420A>T",
"hgvs_p": "p.Ser474Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293588.1",
"strand": false,
"transcript": "XM_047437632.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 505,
"aa_ref": "S",
"aa_start": 473,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6146,
"cdna_start": 1574,
"cds_end": null,
"cds_length": 1518,
"cds_start": 1417,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437633.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1417A>T",
"hgvs_p": "p.Ser473Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293589.1",
"strand": false,
"transcript": "XM_047437633.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 504,
"aa_ref": "S",
"aa_start": 472,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6143,
"cdna_start": 1571,
"cds_end": null,
"cds_length": 1515,
"cds_start": 1414,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437634.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1414A>T",
"hgvs_p": "p.Ser472Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293590.1",
"strand": false,
"transcript": "XM_047437634.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 504,
"aa_ref": "S",
"aa_start": 472,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6143,
"cdna_start": 1571,
"cds_end": null,
"cds_length": 1515,
"cds_start": 1414,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437635.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1414A>T",
"hgvs_p": "p.Ser472Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293591.1",
"strand": false,
"transcript": "XM_047437635.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 496,
"aa_ref": "S",
"aa_start": 464,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6119,
"cdna_start": 1547,
"cds_end": null,
"cds_length": 1491,
"cds_start": 1390,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437636.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1390A>T",
"hgvs_p": "p.Ser464Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293592.1",
"strand": false,
"transcript": "XM_047437636.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 495,
"aa_ref": "S",
"aa_start": 463,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6116,
"cdna_start": 1544,
"cds_end": null,
"cds_length": 1488,
"cds_start": 1387,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437637.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1387A>T",
"hgvs_p": "p.Ser463Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293593.1",
"strand": false,
"transcript": "XM_047437637.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 494,
"aa_ref": "S",
"aa_start": 462,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6113,
"cdna_start": 1541,
"cds_end": null,
"cds_length": 1485,
"cds_start": 1384,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437638.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1384A>T",
"hgvs_p": "p.Ser462Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293594.1",
"strand": false,
"transcript": "XM_047437638.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 494,
"aa_ref": "S",
"aa_start": 462,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6113,
"cdna_start": 1541,
"cds_end": null,
"cds_length": 1485,
"cds_start": 1384,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437669.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1384A>T",
"hgvs_p": "p.Ser462Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293625.1",
"strand": false,
"transcript": "XM_047437669.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 493,
"aa_ref": "S",
"aa_start": 461,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6110,
"cdna_start": 1538,
"cds_end": null,
"cds_length": 1482,
"cds_start": 1381,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437671.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1381A>T",
"hgvs_p": "p.Ser461Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293627.1",
"strand": false,
"transcript": "XM_047437671.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 486,
"aa_ref": "S",
"aa_start": 454,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6089,
"cdna_start": 1517,
"cds_end": null,
"cds_length": 1461,
"cds_start": 1360,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437639.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1360A>T",
"hgvs_p": "p.Ser454Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293595.1",
"strand": false,
"transcript": "XM_047437639.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 485,
"aa_ref": "S",
"aa_start": 453,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6086,
"cdna_start": 1514,
"cds_end": null,
"cds_length": 1458,
"cds_start": 1357,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437640.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1357A>T",
"hgvs_p": "p.Ser453Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293596.1",
"strand": false,
"transcript": "XM_047437640.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 485,
"aa_ref": "S",
"aa_start": 453,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6086,
"cdna_start": 1514,
"cds_end": null,
"cds_length": 1458,
"cds_start": 1357,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437641.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1357A>T",
"hgvs_p": "p.Ser453Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293597.1",
"strand": false,
"transcript": "XM_047437641.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 485,
"aa_ref": "S",
"aa_start": 453,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6086,
"cdna_start": 1514,
"cds_end": null,
"cds_length": 1458,
"cds_start": 1357,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437642.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1357A>T",
"hgvs_p": "p.Ser453Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293598.1",
"strand": false,
"transcript": "XM_047437642.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 484,
"aa_ref": "S",
"aa_start": 452,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6083,
"cdna_start": 1511,
"cds_end": null,
"cds_length": 1455,
"cds_start": 1354,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437643.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1354A>T",
"hgvs_p": "p.Ser452Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293599.1",
"strand": false,
"transcript": "XM_047437643.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 484,
"aa_ref": "S",
"aa_start": 452,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6083,
"cdna_start": 1511,
"cds_end": null,
"cds_length": 1455,
"cds_start": 1354,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437644.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1354A>T",
"hgvs_p": "p.Ser452Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293600.1",
"strand": false,
"transcript": "XM_047437644.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 484,
"aa_ref": "S",
"aa_start": 452,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6083,
"cdna_start": 1511,
"cds_end": null,
"cds_length": 1455,
"cds_start": 1354,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437645.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1354A>T",
"hgvs_p": "p.Ser452Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293601.1",
"strand": false,
"transcript": "XM_047437645.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 483,
"aa_ref": "S",
"aa_start": 451,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6080,
"cdna_start": 1508,
"cds_end": null,
"cds_length": 1452,
"cds_start": 1351,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437646.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1351A>T",
"hgvs_p": "p.Ser451Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293602.1",
"strand": false,
"transcript": "XM_047437646.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 476,
"aa_ref": "S",
"aa_start": 444,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6059,
"cdna_start": 1487,
"cds_end": null,
"cds_length": 1431,
"cds_start": 1330,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437653.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1330A>T",
"hgvs_p": "p.Ser444Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293609.1",
"strand": false,
"transcript": "XM_047437653.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 475,
"aa_ref": "S",
"aa_start": 443,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6056,
"cdna_start": 1484,
"cds_end": null,
"cds_length": 1428,
"cds_start": 1327,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437647.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1327A>T",
"hgvs_p": "p.Ser443Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293603.1",
"strand": false,
"transcript": "XM_047437647.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 475,
"aa_ref": "S",
"aa_start": 443,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6056,
"cdna_start": 1484,
"cds_end": null,
"cds_length": 1428,
"cds_start": 1327,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437648.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1327A>T",
"hgvs_p": "p.Ser443Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293604.1",
"strand": false,
"transcript": "XM_047437648.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 475,
"aa_ref": "S",
"aa_start": 443,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6056,
"cdna_start": 1484,
"cds_end": null,
"cds_length": 1428,
"cds_start": 1327,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437670.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1327A>T",
"hgvs_p": "p.Ser443Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293626.1",
"strand": false,
"transcript": "XM_047437670.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 474,
"aa_ref": "S",
"aa_start": 442,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6053,
"cdna_start": 1481,
"cds_end": null,
"cds_length": 1425,
"cds_start": 1324,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437649.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1324A>T",
"hgvs_p": "p.Ser442Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293605.1",
"strand": false,
"transcript": "XM_047437649.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 474,
"aa_ref": "S",
"aa_start": 442,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6053,
"cdna_start": 1481,
"cds_end": null,
"cds_length": 1425,
"cds_start": 1324,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437650.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1324A>T",
"hgvs_p": "p.Ser442Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293606.1",
"strand": false,
"transcript": "XM_047437650.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 474,
"aa_ref": "S",
"aa_start": 442,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6053,
"cdna_start": 1481,
"cds_end": null,
"cds_length": 1425,
"cds_start": 1324,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437651.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1324A>T",
"hgvs_p": "p.Ser442Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293607.1",
"strand": false,
"transcript": "XM_047437651.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 473,
"aa_ref": "S",
"aa_start": 441,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6050,
"cdna_start": 1478,
"cds_end": null,
"cds_length": 1422,
"cds_start": 1321,
"consequences": [
"missense_variant"
],
"exon_count": 13,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "XM_047437652.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1321A>T",
"hgvs_p": "p.Ser441Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293608.1",
"strand": false,
"transcript": "XM_047437652.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 458,
"aa_ref": "S",
"aa_start": 426,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6005,
"cdna_start": 1433,
"cds_end": null,
"cds_length": 1377,
"cds_start": 1276,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "XM_047437654.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1276A>T",
"hgvs_p": "p.Ser426Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293610.1",
"strand": false,
"transcript": "XM_047437654.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 457,
"aa_ref": "S",
"aa_start": 425,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6002,
"cdna_start": 1430,
"cds_end": null,
"cds_length": 1374,
"cds_start": 1273,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "XM_047437655.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1273A>T",
"hgvs_p": "p.Ser425Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293611.1",
"strand": false,
"transcript": "XM_047437655.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 457,
"aa_ref": "S",
"aa_start": 425,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6002,
"cdna_start": 1430,
"cds_end": null,
"cds_length": 1374,
"cds_start": 1273,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "XM_047437656.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1273A>T",
"hgvs_p": "p.Ser425Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293612.1",
"strand": false,
"transcript": "XM_047437656.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 457,
"aa_ref": "S",
"aa_start": 425,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6002,
"cdna_start": 1430,
"cds_end": null,
"cds_length": 1374,
"cds_start": 1273,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "XM_047437657.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1273A>T",
"hgvs_p": "p.Ser425Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293613.1",
"strand": false,
"transcript": "XM_047437657.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 456,
"aa_ref": "S",
"aa_start": 424,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5999,
"cdna_start": 1427,
"cds_end": null,
"cds_length": 1371,
"cds_start": 1270,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "XM_047437658.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1270A>T",
"hgvs_p": "p.Ser424Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293614.1",
"strand": false,
"transcript": "XM_047437658.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 456,
"aa_ref": "S",
"aa_start": 424,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5999,
"cdna_start": 1427,
"cds_end": null,
"cds_length": 1371,
"cds_start": 1270,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "XM_047437659.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1270A>T",
"hgvs_p": "p.Ser424Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293615.1",
"strand": false,
"transcript": "XM_047437659.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 456,
"aa_ref": "S",
"aa_start": 424,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5999,
"cdna_start": 1427,
"cds_end": null,
"cds_length": 1371,
"cds_start": 1270,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "XM_047437660.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1270A>T",
"hgvs_p": "p.Ser424Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293616.1",
"strand": false,
"transcript": "XM_047437660.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 455,
"aa_ref": "S",
"aa_start": 423,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5996,
"cdna_start": 1424,
"cds_end": null,
"cds_length": 1368,
"cds_start": 1267,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "XM_047437661.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1267A>T",
"hgvs_p": "p.Ser423Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293617.1",
"strand": false,
"transcript": "XM_047437661.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 448,
"aa_ref": "S",
"aa_start": 416,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5975,
"cdna_start": 1403,
"cds_end": null,
"cds_length": 1347,
"cds_start": 1246,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "XM_047437662.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1246A>T",
"hgvs_p": "p.Ser416Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293618.1",
"strand": false,
"transcript": "XM_047437662.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 447,
"aa_ref": "S",
"aa_start": 415,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5972,
"cdna_start": 1400,
"cds_end": null,
"cds_length": 1344,
"cds_start": 1243,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "XM_047437663.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1243A>T",
"hgvs_p": "p.Ser415Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293619.1",
"strand": false,
"transcript": "XM_047437663.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 447,
"aa_ref": "S",
"aa_start": 415,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5972,
"cdna_start": 1400,
"cds_end": null,
"cds_length": 1344,
"cds_start": 1243,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "XM_047437664.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1243A>T",
"hgvs_p": "p.Ser415Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293620.1",
"strand": false,
"transcript": "XM_047437664.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 447,
"aa_ref": "S",
"aa_start": 415,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5972,
"cdna_start": 1400,
"cds_end": null,
"cds_length": 1344,
"cds_start": 1243,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "XM_047437665.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1243A>T",
"hgvs_p": "p.Ser415Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293621.1",
"strand": false,
"transcript": "XM_047437665.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 446,
"aa_ref": "S",
"aa_start": 414,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5969,
"cdna_start": 1397,
"cds_end": null,
"cds_length": 1341,
"cds_start": 1240,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "XM_047437666.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1240A>T",
"hgvs_p": "p.Ser414Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293622.1",
"strand": false,
"transcript": "XM_047437666.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 446,
"aa_ref": "S",
"aa_start": 414,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5969,
"cdna_start": 1397,
"cds_end": null,
"cds_length": 1341,
"cds_start": 1240,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "XM_047437667.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1240A>T",
"hgvs_p": "p.Ser414Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293623.1",
"strand": false,
"transcript": "XM_047437667.1",
"transcript_support_level": null
},
{
"aa_alt": "C",
"aa_end": null,
"aa_length": 446,
"aa_ref": "S",
"aa_start": 414,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5969,
"cdna_start": 1397,
"cds_end": null,
"cds_length": 1341,
"cds_start": 1240,
"consequences": [
"missense_variant"
],
"exon_count": 12,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "XM_047437668.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "c.1240A>T",
"hgvs_p": "p.Ser414Cys",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047293624.1",
"strand": false,
"transcript": "XM_047437668.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 579,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 2,
"exon_rank": 1,
"exon_rank_end": null,
"feature": "ENST00000590011.1",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "n.70A>T",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": false,
"transcript": "ENST00000590011.1",
"transcript_support_level": 2
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 3236,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 10,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000590112.5",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "n.*1702A>T",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000468428.1",
"strand": false,
"transcript": "ENST00000590112.5",
"transcript_support_level": 2
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 3788,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 13,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NR_148518.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "n.1400A>T",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": false,
"transcript": "NR_148518.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 3785,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 13,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "NR_148519.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "n.1397A>T",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": false,
"transcript": "NR_148519.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 3899,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 14,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NR_148520.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "n.1511A>T",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": false,
"transcript": "NR_148520.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 3902,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 14,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NR_148521.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "n.1514A>T",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": false,
"transcript": "NR_148521.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 3869,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 14,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NR_148522.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "n.1481A>T",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": false,
"transcript": "NR_148522.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 3875,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 14,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NR_148523.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "n.1487A>T",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": false,
"transcript": "NR_148523.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 3872,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 14,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NR_148524.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "n.1484A>T",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": false,
"transcript": "NR_148524.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 3872,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 14,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NR_148525.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "n.1484A>T",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": false,
"transcript": "NR_148525.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 3902,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 14,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NR_148526.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "n.1514A>T",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": false,
"transcript": "NR_148526.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 3905,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 14,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NR_148527.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "n.1517A>T",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": false,
"transcript": "NR_148527.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 3902,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 14,
"exon_rank": 12,
"exon_rank_end": null,
"feature": "NR_148528.2",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "n.1514A>T",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": false,
"transcript": "NR_148528.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "nonsense_mediated_decay",
"canonical": false,
"cdna_end": null,
"cdna_length": 3236,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"3_prime_UTR_variant"
],
"exon_count": 10,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000590112.5",
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"hgvs_c": "n.*1702A>T",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": "ENSP00000468428.1",
"strand": false,
"transcript": "ENST00000590112.5",
"transcript_support_level": 2
}
],
"custom_annotations": null,
"dbscsnv_ada_prediction": null,
"dbscsnv_ada_score": null,
"dbsnp": "rs2067198042",
"effect": "missense_variant",
"frequency_reference_population": 0.0000041627236,
"gene_hgnc_id": 14015,
"gene_symbol": "CELF4",
"gnomad_exomes_ac": 6,
"gnomad_exomes_af": 0.00000416272,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_ac": null,
"gnomad_genomes_af": null,
"gnomad_genomes_homalt": null,
"gnomad_mito_heteroplasmic": null,
"gnomad_mito_homoplasmic": null,
"hom_count_reference_population": 0,
"mitotip_prediction": null,
"mitotip_score": null,
"pathogenicity_classification_combined": null,
"phenotype_combined": null,
"phylop100way_prediction": "Uncertain_significance",
"phylop100way_score": 5.867,
"pos": 37253912,
"ref": "T",
"revel_prediction": "Benign",
"revel_score": 0.256,
"splice_prediction_selected": "Benign",
"splice_score_selected": 0.009999999776482582,
"splice_source_selected": "max_spliceai",
"spliceai_max_prediction": "Benign",
"spliceai_max_score": 0.01,
"transcript": "NM_001353740.2"
}
]
}