Canonical Allele Identifier: CA344845132
Gene: USH2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215674451T>A , CM000663.2:g.215674451T>A GRCh38
NC_000001.10:g.215847793T>A , CM000663.1:g.215847793T>A GRCh37
NC_000001.9:g.213914416T>A NCBI36
NG_009497.1:g.753946A>T
NG_009497.2:g.753998A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.13460A>T MANE Select ENSP00000305941.3:p.Tyr4487Phe
ENST00000674083.1:c.13460A>T ENSP00000501296.1:p.Tyr4487Phe
ENST00000307340.7:c.13460A>T ENSP00000305941.3:p.Tyr4487Phe
NM_206933.2:c.13460A>T NP_996816.2:p.Tyr4487Phe
NM_206933.3:c.13460A>T NP_996816.2:p.Tyr4487Phe
NM_206933.4:c.13460A>T MANE Select NP_996816.3:p.Tyr4487Phe