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      "geneNCBI_id": 3909,
      "geneSymbol": "LAMA3",
      "hgvs": [
        "NM_000227.6:c.1881_1884delinsCCT"
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      "proteinEffect": {
        "hgvs": "NP_000218.3:p.Lys627AsnfsTer17"
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      "referenceSequence": "http://reg.genome.network/refseq/RS710810",
      "MANE": {
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        "maneStatus": "MANE Plus Clinical",
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          "Ensembl": {
            "hgvs": "ENST00000269217.11:c.1881_1884delinsCCT"
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          "RefSeq": {
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        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000269217.5:p.Lys627AsnfsTer17"
          },
          "RefSeq": {
            "hgvs": "NP_000218.3:p.Lys627AsnfsTer17"
          }
        }
      }
    },
    {
      "coordinates": [
        {
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          "referenceAllele": "GCTA",
          "start": 6770
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      ],
      "gene": "http://reg.genome.network/gene/GN006483",
      "geneNCBI_id": 3909,
      "geneSymbol": "LAMA3",
      "hgvs": [
        "NM_001127717.4:c.6540_6543delinsCCT"
      ],
      "proteinEffect": {
        "hgvs": "NP_001121189.2:p.Lys2180AsnfsTer17"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS712231"
    },
    {
      "coordinates": [
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          "referenceAllele": "GCTA",
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      ],
      "gene": "http://reg.genome.network/gene/GN006483",
      "geneNCBI_id": 3909,
      "geneSymbol": "LAMA3",
      "hgvs": [
        "NM_001127718.4:c.1713_1716delinsCCT"
      ],
      "proteinEffect": {
        "hgvs": "NP_001121190.2:p.Lys571AsnfsTer17"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS712232"
    },
    {
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      "gene": "http://reg.genome.network/gene/GN006483",
      "geneNCBI_id": 3909,
      "geneSymbol": "LAMA3",
      "hgvs": [
        "NM_198129.4:c.6708_6711delinsCCT"
      ],
      "proteinEffect": {
        "hgvs": "NP_937762.2:p.Lys2236AsnfsTer17"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS729879",
      "MANE": {
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        "maneStatus": "MANE Select",
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        }
      }
    }
  ],
  "type": "nucleotide"
}