{
  "@context": "http://reg.genome.network/schema/allele.jsonld",
  "@id": "http://reg.genome.network/allele/CA415099421",
  "communityStandardTitle": [
    "NM_000033.4(ABCD1):c.653C>T (p.Pro218Leu)"
  ],
  "externalRecords": {
    "ClinVarAlleles": [
      {
        "@id": "http://www.ncbi.nlm.nih.gov/clinvar/?term=577938[alleleid]",
        "alleleId": 577938,
        "preferredName": "NM_000033.4(ABCD1):c.653C>T (p.Pro218Leu)"
      }
    ],
    "ClinVarVariations": [
      {
        "@id": "http://www.ncbi.nlm.nih.gov/clinvar/variation/585358",
        "RCV": [
          "RCV000710404",
          "RCV000787041"
        ],
        "variationId": 585358
      }
    ],
    "MyVariantInfo_hg19": [
      {
        "@id": "http://myvariant.info/v1/variant/chrX:g.152991374C>T?assembly=hg19",
        "id": "chrX:g.152991374C>T"
      }
    ],
    "MyVariantInfo_hg38": [
      {
        "@id": "http://myvariant.info/v1/variant/chrX:g.153725919C>T?assembly=hg38",
        "id": "chrX:g.153725919C>T"
      }
    ],
    "dbSNP": [
      {
        "@id": "http://www.ncbi.nlm.nih.gov/snp/1569540710",
        "rs": 1569540710
      }
    ]
  },
  "genomicAlleles": [
    {
      "chromosome": "X",
      "coordinates": [
        {
          "allele": "T",
          "end": 153725919,
          "referenceAllele": "C",
          "start": 153725918
        }
      ],
      "hgvs": [
        "NC_000023.11:g.153725919C>T",
        "CM000685.2:g.153725919C>T"
      ],
      "referenceGenome": "GRCh38",
      "referenceSequence": "http://reg.genome.network/refseq/RS000071"
    },
    {
      "chromosome": "X",
      "coordinates": [
        {
          "allele": "T",
          "end": 152991374,
          "referenceAllele": "C",
          "start": 152991373
        }
      ],
      "hgvs": [
        "NC_000023.10:g.152991374C>T",
        "CM000685.1:g.152991374C>T"
      ],
      "referenceGenome": "GRCh37",
      "referenceSequence": "http://reg.genome.network/refseq/RS000047"
    },
    {
      "chromosome": "X",
      "coordinates": [
        {
          "allele": "T",
          "end": 152644568,
          "referenceAllele": "C",
          "start": 152644567
        }
      ],
      "hgvs": [
        "NC_000023.9:g.152644568C>T"
      ],
      "referenceGenome": "NCBI36",
      "referenceSequence": "http://reg.genome.network/refseq/RS000023"
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 6052,
          "referenceAllele": "C",
          "start": 6051
        }
      ],
      "hgvs": [
        "NG_009022.2:g.6052C>T"
      ],
      "referenceSequence": "http://reg.genome.network/refseq/RS001385"
    },
    {
      "coordinates": [
        {
          "allele": "A",
          "end": 3828,
          "referenceAllele": "G",
          "start": 3827
        }
      ],
      "hgvs": [
        "NG_023231.1:g.3828G>A"
      ],
      "referenceSequence": "http://reg.genome.network/refseq/RS003724"
    }
  ],
  "transcriptAlleles": [
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 1064,
          "referenceAllele": "C",
          "start": 1063
        }
      ],
      "gene": "http://reg.genome.network/gene/GN000061",
      "geneNCBI_id": 215,
      "geneSymbol": "ABCD1",
      "hgvs": [
        "ENST00000218104.6:c.653C>T"
      ],
      "proteinEffect": {
        "hgvs": "ENSP00000218104.3:p.Pro218Leu",
        "hgvsWellDefined": "ENSP00000218104.3:p.Pro218Leu"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS740393",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000218104.6:c.653C>T"
          },
          "RefSeq": {
            "hgvs": "NM_000033.4:c.653C>T"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000218104.3:p.Pro218Leu"
          },
          "RefSeq": {
            "hgvs": "NP_000024.2:p.Pro218Leu"
          }
        }
      }
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 1052,
          "referenceAllele": "C",
          "start": 1051
        }
      ],
      "gene": "http://reg.genome.network/gene/GN000061",
      "geneNCBI_id": 215,
      "geneSymbol": "ABCD1",
      "hgvs": [
        "ENST00000218104.5:c.653C>T"
      ],
      "proteinEffect": {
        "hgvs": "ENSP00000218104.3:p.Pro218Leu",
        "hgvsWellDefined": "ENSP00000218104.3:p.Pro218Leu"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS248126"
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 103,
          "referenceAllele": "C",
          "start": 102
        }
      ],
      "gene": "http://reg.genome.network/gene/GN000061",
      "geneNCBI_id": 215,
      "geneSymbol": "ABCD1",
      "hgvs": [
        "ENST00000370129.4:c.98C>T"
      ],
      "proteinEffect": {
        "hgvs": "ENSP00000359147.3:p.Pro33Leu",
        "hgvsWellDefined": "ENSP00000359147.3:p.Pro33Leu"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS267891"
    },
    {
      "@id": "http://reg.genome.network/allele/PA891844766",
      "coordinates": [
        {
          "allele": "T",
          "end": 1052,
          "referenceAllele": "C",
          "start": 1051
        }
      ],
      "gene": "http://reg.genome.network/gene/GN000061",
      "geneNCBI_id": 215,
      "geneSymbol": "ABCD1",
      "hgvs": [
        "NM_000033.3:c.653C>T"
      ],
      "proteinEffect": {
        "hgvs": "NP_000024.2:p.Pro218Leu",
        "hgvsWellDefined": "NP_000024.2:p.Pro218Leu"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS006098"
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 1069,
          "referenceAllele": "C",
          "start": 1068
        }
      ],
      "gene": "http://reg.genome.network/gene/GN000061",
      "geneNCBI_id": 215,
      "geneSymbol": "ABCD1",
      "hgvs": [
        "XR_938507.1:n.1069C>T"
      ],
      "referenceSequence": "http://reg.genome.network/refseq/RS133205"
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 1069,
          "referenceAllele": "C",
          "start": 1068
        }
      ],
      "gene": "http://reg.genome.network/gene/GN000061",
      "geneNCBI_id": 215,
      "geneSymbol": "ABCD1",
      "hgvs": [
        "XR_938507.2:n.1069C>T"
      ],
      "referenceSequence": "http://reg.genome.network/refseq/RS611950"
    },
    {
      "@id": "http://reg.genome.network/allele/PA891844766",
      "coordinates": [
        {
          "allele": "T",
          "end": 1064,
          "referenceAllele": "C",
          "start": 1063
        }
      ],
      "gene": "http://reg.genome.network/gene/GN000061",
      "geneNCBI_id": 215,
      "geneSymbol": "ABCD1",
      "hgvs": [
        "NM_000033.4:c.653C>T"
      ],
      "proteinEffect": {
        "hgvs": "NP_000024.2:p.Pro218Leu",
        "hgvsWellDefined": "NP_000024.2:p.Pro218Leu"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS662294",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000218104.6:c.653C>T"
          },
          "RefSeq": {
            "hgvs": "NM_000033.4:c.653C>T"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000218104.3:p.Pro218Leu"
          },
          "RefSeq": {
            "hgvs": "NP_000024.2:p.Pro218Leu"
          }
        }
      }
    }
  ],
  "type": "nucleotide"
}