Canonical Allele Identifier: CA1220619261
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216247121A= , CM000663.2:g.216247121A= GRCh38
NC_000001.10:g.216420463A= , CM000663.1:g.216420463A= GRCh37
NC_000001.9:g.214487086A= NCBI36
NG_009497.1:g.181276T=
NG_009497.2:g.181328T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.2273T= MANE Select ENSP00000305941.3:p.Phe758=
ENST00000674083.1:c.2273T= ENSP00000501296.1:p.Phe758=
ENST00000307340.7:c.2273T= ENSP00000305941.3:p.Phe758=
ENST00000366942.3:c.2273T= ENSP00000355909.3:p.Phe758=
NM_007123.5:c.2273T= NP_009054.5:p.Phe758=
NM_206933.2:c.2273T= NP_996816.2:p.Phe758=
NM_206933.3:c.2273T= NP_996816.2:p.Phe758=
NM_007123.6:c.2273T= NP_009054.6:p.Phe758=
NM_206933.4:c.2273T= MANE Select NP_996816.3:p.Phe758=