Canonical Allele Identifier: CA344865585
Gene: USH2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216247181C>A , CM000663.2:g.216247181C>A GRCh38
NC_000001.10:g.216420523C>A , CM000663.1:g.216420523C>A GRCh37
NC_000001.9:g.214487146C>A NCBI36
NG_009497.1:g.181216G>T
NG_009497.2:g.181268G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.2213G>T MANE Select ENSP00000305941.3:p.Ser738Ile
ENST00000674083.1:c.2213G>T ENSP00000501296.1:p.Ser738Ile
ENST00000307340.7:c.2213G>T ENSP00000305941.3:p.Ser738Ile
ENST00000366942.3:c.2213G>T ENSP00000355909.3:p.Ser738Ile
NM_007123.5:c.2213G>T NP_009054.5:p.Ser738Ile
NM_206933.2:c.2213G>T NP_996816.2:p.Ser738Ile
NM_206933.3:c.2213G>T NP_996816.2:p.Ser738Ile
NM_007123.6:c.2213G>T NP_009054.6:p.Ser738Ile
NM_206933.4:c.2213G>T MANE Select NP_996816.3:p.Ser738Ile