Canonical Allele Identifier: CA2573131592
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1454245
ClinVar RCV Id: RCV001939442
dbSNP Id: rs2102778595

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215798983_215798984insA , CM000663.2:g.215798983_215798984insA GRCh38
NC_000001.10:g.215972325_215972326insA , CM000663.1:g.215972325_215972326insA GRCh37
NC_000001.9:g.214038948_214038949insA NCBI36
NG_009497.1:g.629413_629414insT
NG_009497.2:g.629465_629466insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.9881_9882insT MANE Select ENSP00000305941.3:p.Cys3295LeufsTer?
ENST00000674083.1:c.9881_9882insT ENSP00000501296.1:p.Cys3295LeufsTer?
ENST00000307340.7:c.9881_9882insT ENSP00000305941.3:p.Cys3295LeufsTer?
NM_206933.2:c.9881_9882insT NP_996816.2:p.Cys3295LeufsTer?
NM_206933.3:c.9881_9882insT NP_996816.2:p.Cys3295LeufsTer?
NM_206933.4:c.9881_9882insT MANE Select NP_996816.3:p.Cys3295LeufsTer?