Canonical Allele Identifier: CA344840981
Gene: USH2A HGNC NCBI

Linked Data

COSMIC: COSM361441

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215671136A>T , CM000663.2:g.215671136A>T GRCh38
NC_000001.10:g.215844478A>T , CM000663.1:g.215844478A>T GRCh37
NC_000001.9:g.213911101A>T NCBI36
NG_009497.1:g.757261T>A
NG_009497.2:g.757313T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.13969T>A MANE Select ENSP00000305941.3:p.Trp4657Arg
ENST00000674083.1:c.13969T>A ENSP00000501296.1:p.Trp4657Arg
ENST00000307340.7:c.13969T>A ENSP00000305941.3:p.Trp4657Arg
NM_206933.2:c.13969T>A NP_996816.2:p.Trp4657Arg
NM_206933.3:c.13969T>A NP_996816.2:p.Trp4657Arg
NM_206933.4:c.13969T>A MANE Select NP_996816.3:p.Trp4657Arg