Canonical Allele Identifier: CA1220416695

Gene: USH2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215782090T= , CM000663.2:g.215782090T=	GRCh38
NC_000001.10:g.215955432T= , CM000663.1:g.215955432T=	GRCh37
NC_000001.9:g.214022055T=	NCBI36
NG_009497.1:g.646307A=
NG_009497.2:g.646359A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000307340.8:c.10692A= MANE Select	ENSP00000305941.3:p.Ser3564=
ENST00000674083.1:c.10692A=	ENSP00000501296.1:p.Ser3564=
ENST00000307340.7:c.10692A=	ENSP00000305941.3:p.Ser3564=
NM_206933.2:c.10692A=	NP_996816.2:p.Ser3564=
NM_206933.3:c.10692A=	NP_996816.2:p.Ser3564=
NM_206933.4:c.10692A= MANE Select	NP_996816.3:p.Ser3564=