Canonical Allele Identifier: CA2275255477

Gene: USH1G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74920175C= , CM000679.2:g.74920175C=	GRCh38
NC_000017.10:g.72916270C= , CM000679.1:g.72916270C=	GRCh37
NC_000017.9:g.70427865C=	NCBI36
NG_007882.1:g.8082G=
NG_033062.1:g.901C=
NG_007882.2:g.8089G=
NG_033062.2:g.901C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.661G= MANE Select	ENSP00000480279.1:p.Glu221=
ENST00000579243.1:c.*260G=	ENSP00000462568.1:n.*260G=
ENST00000614341.4:c.661G=	ENSP00000480279.1:p.Glu221=
NM_001282489.2:c.352G=	NP_001269418.1:p.Glu118=
NM_173477.4:c.661G=	NP_775748.2:p.Glu221=
XM_011524296.1:c.352G=	XP_011522598.1:p.Glu118=
XM_011524296.2:c.352G=	XP_011522598.1:p.Glu118=
NM_173477.5:c.661G= MANE Select	NP_775748.2:p.Glu221=
NM_001282489.3:c.352G=	NP_001269418.1:p.Glu118=