Canonical Allele Identifier: CA2275255416

Gene: USH1G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74920067G= , CM000679.2:g.74920067G=	GRCh38
NC_000017.10:g.72916162G= , CM000679.1:g.72916162G=	GRCh37
NC_000017.9:g.70427757G=	NCBI36
NG_007882.1:g.8190C=
NG_033062.1:g.793G=
NG_007882.2:g.8197C=
NG_033062.2:g.793G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.769C= MANE Select	ENSP00000480279.1:p.Arg257=
ENST00000579243.1:c.*368C=	ENSP00000462568.1:n.*368C=
ENST00000614341.4:c.769C=	ENSP00000480279.1:p.Arg257=
NM_001282489.2:c.460C=	NP_001269418.1:p.Arg154=
NM_173477.4:c.769C=	NP_775748.2:p.Arg257=
XM_011524296.1:c.460C=	XP_011522598.1:p.Arg154=
XM_011524296.2:c.460C=	XP_011522598.1:p.Arg154=
NM_173477.5:c.769C= MANE Select	NP_775748.2:p.Arg257=
NM_001282489.3:c.460C=	NP_001269418.1:p.Arg154=