Canonical Allele Identifier: CA2573132757
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1374473
ClinVar RCV Id: RCV001877846
dbSNP Id: rs2102545129
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216246681del , CM000663.2:g.216246681del GRCh38
NC_000001.10:g.216420023del , CM000663.1:g.216420023del GRCh37
NC_000001.9:g.214486646del NCBI36
NG_009497.1:g.181717del
NG_009497.2:g.181769del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.2714del MANE Select ENSP00000305941.3:p.Leu905TrpfsTer?
ENST00000674083.1:c.2714del ENSP00000501296.1:p.Leu905TrpfsTer?
ENST00000307340.7:c.2714del ENSP00000305941.3:p.Leu905TrpfsTer?
ENST00000366942.3:c.2714del ENSP00000355909.3:p.Leu905TrpfsTer?
NM_007123.5:c.2714del NP_009054.5:p.Leu905TrpfsTer?
NM_206933.2:c.2714del NP_996816.2:p.Leu905TrpfsTer?
NM_206933.3:c.2714del NP_996816.2:p.Leu905TrpfsTer?
NM_007123.6:c.2714del NP_009054.6:p.Leu905TrpfsTer?
NM_206933.4:c.2714del MANE Select NP_996816.3:p.Leu905TrpfsTer?
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