{
  "@context": "http://reg.genome.network/schema/allele.jsonld",
  "@id": "http://reg.genome.network/allele/CA16040997",
  "communityStandardTitle": [
    "NM_000112.4(SLC26A2):c.1537_1541dup (p.Ile514MetfsTer14)"
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      }
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        "RCV": [
          "RCV000409678",
          "RCV000409864",
          "RCV000410828",
          "RCV000412349",
          "RCV001850977"
        ],
        "variationId": 371758
      }
    ],
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      {
        "@id": "http://myvariant.info/v1/variant/chr5:g.149360693_149360697dupGTTAT?assembly=hg19",
        "id": "chr5:g.149360693_149360697dupGTTAT"
      },
      {
        "@id": "http://myvariant.info/v1/variant/chr5:g.149360692_149360693insGTTAT?assembly=hg19",
        "id": "chr5:g.149360692_149360693insGTTAT"
      }
    ],
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      {
        "@id": "http://myvariant.info/v1/variant/chr5:g.149981130_149981134dupGTTAT?assembly=hg38",
        "id": "chr5:g.149981130_149981134dupGTTAT"
      },
      {
        "@id": "http://myvariant.info/v1/variant/chr5:g.149981129_149981130insGTTAT?assembly=hg38",
        "id": "chr5:g.149981129_149981130insGTTAT"
      }
    ],
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        "@id": "http://www.ncbi.nlm.nih.gov/snp/1057517511",
        "rs": 1057517511
      }
    ],
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        "@id": "http://gnomad.broadinstitute.org/variant/5-149360692-A-AGTTAT?dataset=gnomad_r2_1",
        "id": "5-149360692-A-AGTTAT",
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      }
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      {
        "@id": "http://gnomad.broadinstitute.org/variant/5-149981129-A-AGTTAT?dataset=gnomad_r4",
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      }
    ]
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          "referenceAllele": "",
          "start": 149981134
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    },
    {
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          "referenceAllele": "",
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      "referenceSequence": "http://reg.genome.network/refseq/RS000029"
    },
    {
      "chromosome": "5",
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          "referenceAllele": "",
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    },
    {
      "coordinates": [
        {
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      "referenceSequence": "http://reg.genome.network/refseq/RS000500"
    }
  ],
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        "maneStatus": "MANE Select",
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      },
      "referenceSequence": "http://reg.genome.network/refseq/RS253352"
    },
    {
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          "endIntronDirection": "+",
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      ],
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        "hgvs": "ENSP00000426053.1:n.372+2779_372+2783dup"
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        "hgvsWellDefined": "NP_000103.2:p.[Ile514_Thr518del;Ser522_Ala523delinsGly;Ser526_Gly530del;Leu532_Val535delinsCys;Phe537_Phe540delinsProLeuHis;Val542_Ile543del]"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS006175"
    },
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      "hgvs": [
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      ],
      "proteinEffect": {
        "hgvs": "XP_016864680.1:p.Ile514MetfsTer14",
        "hgvsWellDefined": "XP_016864680.1:p.[Ile514_Thr518del;Ser522_Ala523delinsGly;Ser526_Gly530del;Leu532_Val535delinsCys;Phe537_Phe540delinsProLeuHis;Val542_Ile543del]"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS563549"
    },
    {
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      "proteinEffect": {
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        "hgvsWellDefined": "NP_000103.2:p.[Ile514_Thr518del;Ser522_Ala523delinsGly;Ser526_Gly530del;Leu532_Val535delinsCys;Phe537_Phe540delinsProLeuHis;Val542_Ile543del]"
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      "referenceSequence": "http://reg.genome.network/refseq/RS674707",
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        "maneStatus": "MANE Select",
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          "Ensembl": {
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          },
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            "hgvs": "NP_000103.2:p.Ile514MetfsTer14"
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        }
      }
    }
  ],
  "type": "nucleotide"
}