{
  "@context": "http://reg.genome.network/schema/allele.jsonld",
  "@id": "http://reg.genome.network/allele/CA213328",
  "communityStandardTitle": [
    "NM_139058.3(ARX):c.409dup (p.Glu137GlyfsTer?)"
  ],
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      }
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      {
        "@id": "http://www.ncbi.nlm.nih.gov/clinvar/variation/210330",
        "RCV": [
          "RCV000192991"
        ],
        "variationId": 210330
      }
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      {
        "@id": "http://myvariant.info/v1/variant/chrX:g.25031703dupC?assembly=hg19",
        "id": "chrX:g.25031703dupC"
      },
      {
        "@id": "http://myvariant.info/v1/variant/chrX:g.25031702_25031703insC?assembly=hg19",
        "id": "chrX:g.25031702_25031703insC"
      }
    ],
    "MyVariantInfo_hg38": [
      {
        "@id": "http://myvariant.info/v1/variant/chrX:g.25013586dupC?assembly=hg38",
        "id": "chrX:g.25013586dupC"
      },
      {
        "@id": "http://myvariant.info/v1/variant/chrX:g.25013585_25013586insC?assembly=hg38",
        "id": "chrX:g.25013585_25013586insC"
      }
    ],
    "dbSNP": [
      {
        "@id": "http://www.ncbi.nlm.nih.gov/snp/797045298",
        "rs": 797045298
      }
    ]
  },
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    {
      "chromosome": "X",
      "coordinates": [
        {
          "allele": "C",
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          "referenceAllele": "",
          "start": 25013589
        }
      ],
      "hgvs": [
        "NC_000023.11:g.25013589dup",
        "CM000685.2:g.25013589dup"
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      "referenceGenome": "GRCh38",
      "referenceSequence": "http://reg.genome.network/refseq/RS000071"
    },
    {
      "chromosome": "X",
      "coordinates": [
        {
          "allele": "C",
          "end": 25031706,
          "referenceAllele": "",
          "start": 25031706
        }
      ],
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        "CM000685.1:g.25031706dup"
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      "referenceGenome": "GRCh37",
      "referenceSequence": "http://reg.genome.network/refseq/RS000047"
    },
    {
      "chromosome": "X",
      "coordinates": [
        {
          "allele": "C",
          "end": 24941627,
          "referenceAllele": "",
          "start": 24941627
        }
      ],
      "hgvs": [
        "NC_000023.9:g.24941627dup"
      ],
      "referenceGenome": "NCBI36",
      "referenceSequence": "http://reg.genome.network/refseq/RS000023"
    },
    {
      "coordinates": [
        {
          "allele": "G",
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          "referenceAllele": "",
          "start": 7363
        }
      ],
      "hgvs": [
        "NG_008281.1:g.7363dup"
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      "referenceSequence": "http://reg.genome.network/refseq/RS000995"
    }
  ],
  "transcriptAlleles": [
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          "end": 637,
          "referenceAllele": "",
          "start": 637
        }
      ],
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      "geneNCBI_id": 170302,
      "geneSymbol": "ARX",
      "hgvs": [
        "ENST00000379044.5:c.409dup"
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      },
      "referenceSequence": "http://reg.genome.network/refseq/RS752163",
      "MANE": {
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        "maneStatus": "MANE Select",
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        },
        "protein": {
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            "hgvs": "ENSP00000368332.4:p.Glu137GlyfsTer?"
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            "hgvs": "NP_620689.1:p.Glu137GlyfsTer?"
          }
        }
      }
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    {
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      "geneNCBI_id": 170302,
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      },
      "referenceSequence": "http://reg.genome.network/refseq/RS272310"
    },
    {
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          "referenceAllele": "",
          "start": 620
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      "geneSymbol": "ARX",
      "hgvs": [
        "NM_139058.2:c.409dup"
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      "proteinEffect": {
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        "hgvsWellDefined": "NP_620689.1:p.[Glu137_Gly141delinsGlyThr;Ala144_Thr158delinsArgArgArgGlyArgArgGlySerArgGlyArgGlyArgArgGly;Lys160_Ser162delinsGlyHisAla;Ala164delinsAspGln;Gln166delinsGlyAlaAla]"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS040971"
    },
    {
      "coordinates": [
        {
          "allele": "G",
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          "referenceAllele": "",
          "start": 637
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      ],
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      "geneSymbol": "ARX",
      "hgvs": [
        "NM_139058.3:c.409dup"
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      "proteinEffect": {
        "hgvs": "NP_620689.1:p.Glu137GlyfsTer?",
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      },
      "referenceSequence": "http://reg.genome.network/refseq/RS671983",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
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          "RefSeq": {
            "hgvs": "NM_139058.3:c.409dup"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000368332.4:p.Glu137GlyfsTer?"
          },
          "RefSeq": {
            "hgvs": "NP_620689.1:p.Glu137GlyfsTer?"
          }
        }
      }
    }
  ],
  "type": "nucleotide"
}