Canonical Allele Identifier: CA2275255460

Gene: USH1G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74920141T= , CM000679.2:g.74920141T=	GRCh38
NC_000017.10:g.72916236T= , CM000679.1:g.72916236T=	GRCh37
NC_000017.9:g.70427831T=	NCBI36
NG_007882.1:g.8116A=
NG_033062.1:g.867T=
NG_007882.2:g.8123A=
NG_033062.2:g.867T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.695A= MANE Select	ENSP00000480279.1:p.Lys232=
ENST00000579243.1:c.*294A=	ENSP00000462568.1:n.*294A=
ENST00000614341.4:c.695A=	ENSP00000480279.1:p.Lys232=
NM_001282489.2:c.386A=	NP_001269418.1:p.Lys129=
NM_173477.4:c.695A=	NP_775748.2:p.Lys232=
XM_011524296.1:c.386A=	XP_011522598.1:p.Lys129=
XM_011524296.2:c.386A=	XP_011522598.1:p.Lys129=
NM_173477.5:c.695A= MANE Select	NP_775748.2:p.Lys232=
NM_001282489.3:c.386A=	NP_001269418.1:p.Lys129=