Canonical Allele Identifier: CA1220372153

Gene: USH2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215671088A= , CM000663.2:g.215671088A=	GRCh38
NC_000001.10:g.215844430A= , CM000663.1:g.215844430A=	GRCh37
NC_000001.9:g.213911053A=	NCBI36
NG_009497.1:g.757309T=
NG_009497.2:g.757361T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.14017T= MANE Select	ENSP00000305941.3:p.Tyr4673=
ENST00000674083.1:c.14017T=	ENSP00000501296.1:p.Tyr4673=
ENST00000307340.7:c.14017T=	ENSP00000305941.3:p.Tyr4673=
NM_206933.2:c.14017T=	NP_996816.2:p.Tyr4673=
NM_206933.3:c.14017T=	NP_996816.2:p.Tyr4673=
NM_206933.4:c.14017T= MANE Select	NP_996816.3:p.Tyr4673=