Canonical Allele Identifier: CA1220652958

Gene: USH2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.216325511G= , CM000663.2:g.216325511G=	GRCh38
NC_000001.10:g.216498853G= , CM000663.1:g.216498853G=	GRCh37
NC_000001.9:g.214565476G=	NCBI36
NG_009497.1:g.102886C=
NG_009497.2:g.102938C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000307340.8:c.937C= MANE Select	ENSP00000305941.3:p.Pro313=
ENST00000674083.1:c.937C=	ENSP00000501296.1:p.Pro313=
ENST00000307340.7:c.937C=	ENSP00000305941.3:p.Pro313=
ENST00000366942.3:c.937C=	ENSP00000355909.3:p.Pro313=
NM_007123.5:c.937C=	NP_009054.5:p.Pro313=
NM_206933.2:c.937C=	NP_996816.2:p.Pro313=
NM_206933.3:c.937C=	NP_996816.2:p.Pro313=
NM_007123.6:c.937C=	NP_009054.6:p.Pro313=
NM_206933.4:c.937C= MANE Select	NP_996816.3:p.Pro313=