Canonical Allele Identifier: CA1220426279

Gene: USH2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.215799104T= , CM000663.2:g.215799104T=	GRCh38
NC_000001.10:g.215972446T= , CM000663.1:g.215972446T=	GRCh37
NC_000001.9:g.214039069T=	NCBI36
NG_009497.1:g.629293A=
NG_009497.2:g.629345A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.9761A= MANE Select	ENSP00000305941.3:p.Glu3254=
ENST00000674083.1:c.9761A=	ENSP00000501296.1:p.Glu3254=
ENST00000307340.7:c.9761A=	ENSP00000305941.3:p.Glu3254=
NM_206933.2:c.9761A=	NP_996816.2:p.Glu3254=
NM_206933.3:c.9761A=	NP_996816.2:p.Glu3254=
NM_206933.4:c.9761A= MANE Select	NP_996816.3:p.Glu3254=