← 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: 18-36133317-G-GT (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=18&pos=36133317&ref=G&alt=GT&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 0,
          "criteria": [
            "PVS1_Moderate"
          ],
          "effects": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "gene_symbol": "ELP2",
          "hgnc_id": 18248,
          "hgvs_c": "c.",
          "hgvs_p": null,
          "inheritance_mode": "AR",
          "pathogenic_score": 2,
          "score": 2,
          "transcript": "ENST00000358232.11",
          "verdict": "Uncertain_significance"
        }
      ],
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PVS1_Moderate",
      "acmg_score": 2,
      "allele_count_reference_population": 0,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "TG",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": null,
      "bayesdelnoaf_score": null,
      "chr": "18",
      "clinvar_classification": "",
      "clinvar_disease": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "computational_prediction_selected": null,
      "computational_score_selected": null,
      "computational_source_selected": null,
      "consequences": [
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 826,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 8432,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2481,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 22,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000358232.11",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_018255.4",
          "protein_coding": true,
          "protein_id": "ENSP00000350967.6",
          "strand": true,
          "transcript": "ENST00000358232.11",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 756,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2385,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2271,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 19,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000423854.6",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000391202.2",
          "strand": true,
          "transcript": "ENST00000423854.6",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 756,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2288,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2271,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 20,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000542824.5",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000443800.1",
          "strand": true,
          "transcript": "ENST00000542824.5",
          "transcript_support_level": 1
        },
        {
          "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": 2542,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 22,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000539560.5",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "n.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000443555.1",
          "strand": true,
          "transcript": "ENST00000539560.5",
          "transcript_support_level": 1
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 56,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 535,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 172,
          "cds_start": null,
          "consequences": [
            "splice_region_variant",
            "exon_region"
          ],
          "exon_count": 7,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000543127.5",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000440426.1",
          "strand": true,
          "transcript": "ENST00000543127.5",
          "transcript_support_level": 4
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 898,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2728,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2697,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 23,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000867817.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000537876.1",
          "strand": true,
          "transcript": "ENST00000867817.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 891,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2722,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2676,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 23,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000442325.6",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000414851.2",
          "strand": true,
          "transcript": "ENST00000442325.6",
          "transcript_support_level": 2
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 889,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5977,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2670,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 23,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000867807.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000537866.1",
          "strand": true,
          "transcript": "ENST00000867807.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 885,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2704,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2658,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 23,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000965732.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000635791.1",
          "strand": true,
          "transcript": "ENST00000965732.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 865,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2653,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2598,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 22,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000867812.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000537871.1",
          "strand": true,
          "transcript": "ENST00000867812.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 853,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2604,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2562,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 23,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000965733.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000635792.1",
          "strand": true,
          "transcript": "ENST00000965733.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 847,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2579,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2544,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 22,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000867816.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000537875.1",
          "strand": true,
          "transcript": "ENST00000867816.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 847,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2562,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2544,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 21,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000867822.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000537881.1",
          "strand": true,
          "transcript": "ENST00000867822.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 845,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3800,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2538,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 23,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000965728.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000635787.1",
          "strand": true,
          "transcript": "ENST00000965728.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 841,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5849,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2526,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 22,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000867805.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000537864.1",
          "strand": true,
          "transcript": "ENST00000867805.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 833,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2542,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2502,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 22,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000939573.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000609632.1",
          "strand": true,
          "transcript": "ENST00000939573.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 829,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2509,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2490,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 22,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000867821.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000537880.1",
          "strand": true,
          "transcript": "ENST00000867821.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 824,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5788,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2475,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 22,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000867806.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000537865.1",
          "strand": true,
          "transcript": "ENST00000867806.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 824,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2525,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2475,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 22,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000867814.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000537873.1",
          "strand": true,
          "transcript": "ENST00000867814.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 823,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2520,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2472,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 22,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000867815.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000537874.1",
          "strand": true,
          "transcript": "ENST00000867815.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 821,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2487,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2466,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 21,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000350494.10",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000316051.6",
          "strand": true,
          "transcript": "ENST00000350494.10",
          "transcript_support_level": 2
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 807,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2534,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2424,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 22,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000965731.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000635790.1",
          "strand": true,
          "transcript": "ENST00000965731.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 806,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2510,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2421,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 22,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000867810.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000537869.1",
          "strand": true,
          "transcript": "ENST00000867810.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 801,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2455,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2406,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 22,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000939570.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000609629.1",
          "strand": true,
          "transcript": "ENST00000939570.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 800,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2453,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2403,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 21,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000351393.10",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000257191.7",
          "strand": true,
          "transcript": "ENST00000351393.10",
          "transcript_support_level": 2
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 798,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2509,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2397,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 21,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000867808.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000537867.1",
          "strand": true,
          "transcript": "ENST00000867808.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 798,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3856,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2397,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 21,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000965727.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000635786.1",
          "strand": true,
          "transcript": "ENST00000965727.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 788,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2452,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2367,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 21,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000867811.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000537870.1",
          "strand": true,
          "transcript": "ENST00000867811.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 782,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5677,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2349,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 21,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000867804.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000537863.1",
          "strand": true,
          "transcript": "ENST00000867804.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 782,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2401,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2349,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 20,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000867813.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000537872.1",
          "strand": true,
          "transcript": "ENST00000867813.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 779,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2361,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2340,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 21,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000867820.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000537879.1",
          "strand": true,
          "transcript": "ENST00000867820.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 776,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2435,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2331,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 21,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000867809.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000537868.1",
          "strand": true,
          "transcript": "ENST00000867809.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 764,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5617,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2295,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 21,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000939564.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000609623.1",
          "strand": true,
          "transcript": "ENST00000939564.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 763,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5613,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2292,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 21,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000939565.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000609624.1",
          "strand": true,
          "transcript": "ENST00000939565.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 743,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2270,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2232,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 21,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000965734.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000635793.1",
          "strand": true,
          "transcript": "ENST00000965734.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 738,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3449,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2217,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 21,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000939568.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000609627.1",
          "strand": true,
          "transcript": "ENST00000939568.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 736,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5542,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2211,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 21,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000939562.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000609621.1",
          "strand": true,
          "transcript": "ENST00000939562.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 721,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5481,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2166,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 20,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000939566.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000609625.1",
          "strand": true,
          "transcript": "ENST00000939566.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 720,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2210,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2163,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 20,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000939571.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000609630.1",
          "strand": true,
          "transcript": "ENST00000939571.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 719,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2179,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2160,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 20,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000939576.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000609635.1",
          "strand": true,
          "transcript": "ENST00000939576.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 717,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 3421,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2154,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 20,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000939567.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000609626.1",
          "strand": true,
          "transcript": "ENST00000939567.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 712,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2183,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2139,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 20,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000939572.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000609631.1",
          "strand": true,
          "transcript": "ENST00000939572.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 712,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2174,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2139,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 18,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000939574.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000609633.1",
          "strand": true,
          "transcript": "ENST00000939574.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 712,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2252,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2139,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 18,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000965730.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000635789.1",
          "strand": true,
          "transcript": "ENST00000965730.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 710,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5455,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2133,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 20,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000939563.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000609622.1",
          "strand": true,
          "transcript": "ENST00000939563.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 709,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2153,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2130,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 18,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000867819.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000537878.1",
          "strand": true,
          "transcript": "ENST00000867819.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 686,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2099,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 2061,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 18,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000965735.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000635794.1",
          "strand": true,
          "transcript": "ENST00000965735.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 652,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2078,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 1959,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 18,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000939569.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000609628.1",
          "strand": true,
          "transcript": "ENST00000939569.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 647,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1968,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 1944,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 17,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000867818.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000537877.1",
          "strand": true,
          "transcript": "ENST00000867818.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 608,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1941,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 1827,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 17,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000965729.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000635788.1",
          "strand": true,
          "transcript": "ENST00000965729.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 557,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 1693,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 1674,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 16,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000939575.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000609634.1",
          "strand": true,
          "transcript": "ENST00000939575.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": 56,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 535,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": 172,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "5_prime_UTR_variant",
            "intron_variant"
          ],
          "exon_count": 7,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000543127.5",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "c.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000440426.1",
          "strand": true,
          "transcript": "ENST00000543127.5",
          "transcript_support_level": 4
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": null,
          "canonical": null,
          "cdna_end": null,
          "cdna_length": null,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "intragenic_variant"
          ],
          "exon_count": null,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": null,
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "n.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": null,
          "protein_id": null,
          "strand": true,
          "transcript": null,
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "retained_intron",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 692,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 4,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000535488.5",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "n.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": true,
          "transcript": "ENST00000535488.5",
          "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": 575,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 5,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000540135.5",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "n.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": true,
          "transcript": "ENST00000540135.5",
          "transcript_support_level": 3
        },
        {
          "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": 381,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 5,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000540799.1",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "n.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000468091.1",
          "strand": true,
          "transcript": "ENST00000540799.1",
          "transcript_support_level": 3
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "retained_intron",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 583,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 3,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000541190.5",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "n.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": true,
          "transcript": "ENST00000541190.5",
          "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": 649,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "splice_donor_variant",
            "splice_region_variant",
            "intron_variant",
            "exon_region"
          ],
          "exon_count": 7,
          "exon_rank": 2,
          "exon_rank_end": null,
          "feature": "ENST00000542430.5",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "n.",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000440774.1",
          "strand": true,
          "transcript": "ENST00000542430.5",
          "transcript_support_level": 5
        },
        {
          "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": 553,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 5,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000544267.5",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "n.",
          "hgvs_p": null,
          "intron_rank": 1,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000440516.1",
          "strand": true,
          "transcript": "ENST00000544267.5",
          "transcript_support_level": 4
        },
        {
          "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": 569,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 6,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000545632.5",
          "gene_hgnc_id": 18248,
          "gene_symbol": "ELP2",
          "hgvs_c": "n.",
          "hgvs_p": null,
          "intron_rank": 1,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": "ENSP00000438533.1",
          "strand": true,
          "transcript": "ENST00000545632.5",
          "transcript_support_level": 4
        }
      ],
      "custom_annotations": null,
      "dbscsnv_ada_prediction": null,
      "dbscsnv_ada_score": null,
      "dbsnp": null,
      "effect": "splice_donor_variant,splice_region_variant,intron_variant,exon_region",
      "frequency_reference_population": null,
      "gene_hgnc_id": 18248,
      "gene_symbol": "ELP2",
      "gnomad_exomes_ac": null,
      "gnomad_exomes_af": null,
      "gnomad_exomes_homalt": null,
      "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": 4.658,
      "pos": 36133316,
      "ref": "TG",
      "revel_prediction": null,
      "revel_score": null,
      "splice_prediction_selected": null,
      "splice_score_selected": null,
      "splice_source_selected": null,
      "spliceai_max_prediction": null,
      "spliceai_max_score": null,
      "transcript": "ENST00000358232.11"
    }
  ]
}
For research and educational, non-commercial use only. Not for clinical or diagnostic use. GeneBe does not provide medical advice. Data use for AI modeling is prohibited: if used, the cost is $0.001 per byte of downloaded uncompressed data.