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        "hgvs": "NP_001157979.2:p.Asn8520GlnfsTer4",
        "hgvsWellDefined": "NP_001157979.2:p.Asn8520_Ile8525delinsGlnLeuArg"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS713104",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Plus Clinical",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000427231.7:c.25557dup"
          },
          "RefSeq": {
            "hgvs": "NM_001164507.2:c.25557dup"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000416578.2:p.Asn8520GlnfsTer4"
          },
          "RefSeq": {
            "hgvs": "NP_001157979.2:p.Asn8520GlnfsTer4"
          }
        }
      }
    },
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 25749,
          "referenceAllele": "",
          "start": 25749
        }
      ],
      "gene": "http://reg.genome.network/gene/GN007720",
      "geneNCBI_id": 4703,
      "geneSymbol": "NEB",
      "hgvs": [
        "NM_001164508.2:c.25557dup"
      ],
      "proteinEffect": {
        "hgvs": "NP_001157980.2:p.Asn8520GlnfsTer4",
        "hgvsWellDefined": "NP_001157980.2:p.Asn8520_Ile8525delinsGlnLeuArg"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS713105",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000397345.8:c.25557dup"
          },
          "RefSeq": {
            "hgvs": "NM_001164508.2:c.25557dup"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000380505.3:p.Asn8520GlnfsTer4"
          },
          "RefSeq": {
            "hgvs": "NP_001157980.2:p.Asn8520GlnfsTer4"
          }
        }
      }
    }
  ],
  "type": "nucleotide"
}