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      "hgvs": [
        "XM_011515754.1:c.2796del"
      ],
      "proteinEffect": {
        "hgvs": "XP_011514056.1:p.Tyr933ThrfsTer9",
        "hgvsWellDefined": "XP_011514056.1:p.[Tyr933_Ala937del;Val939_Met947delinsSer;Arg949_Phe952del;Thr955_Ser956del;Gln958_Lys960delinsCys;Leu962del]"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS082965"
    },
    {
      "coordinates": [
        {
          "allele": "",
          "end": 3109,
          "referenceAllele": "C",
          "start": 3108
        }
      ],
      "gene": "http://reg.genome.network/gene/GN001884",
      "geneNCBI_id": 1080,
      "geneSymbol": "CFTR",
      "hgvs": [
        "NM_000492.4:c.3039del"
      ],
      "proteinEffect": {
        "hgvs": "NP_000483.3:p.Tyr1014ThrfsTer9",
        "hgvsWellDefined": "NP_000483.3:p.[Tyr1014_Ala1018del;Val1020_Met1028delinsSer;Arg1030_Phe1033del;Thr1036_Ser1037del;Gln1039_Lys1041delinsCys;Leu1043del]"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS674867",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000003084.11:c.3039del"
          },
          "RefSeq": {
            "hgvs": "NM_000492.4:c.3039del"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000003084.6:p.Tyr1014ThrfsTer9"
          },
          "RefSeq": {
            "hgvs": "NP_000483.3:p.Tyr1014ThrfsTer9"
          }
        }
      }
    }
  ],
  "type": "nucleotide"
}