Canonical Allele Identifier: CA2275255475

Gene: USH1G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74920171C= , CM000679.2:g.74920171C=	GRCh38
NC_000017.10:g.72916266C= , CM000679.1:g.72916266C=	GRCh37
NC_000017.9:g.70427861C=	NCBI36
NG_007882.1:g.8086G=
NG_033062.1:g.897C=
NG_007882.2:g.8093G=
NG_033062.2:g.897C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.665G= MANE Select	ENSP00000480279.1:p.Arg222=
ENST00000579243.1:c.*264G=	ENSP00000462568.1:n.*264G=
ENST00000614341.4:c.665G=	ENSP00000480279.1:p.Arg222=
NM_001282489.2:c.356G=	NP_001269418.1:p.Arg119=
NM_173477.4:c.665G=	NP_775748.2:p.Arg222=
XM_011524296.1:c.356G=	XP_011522598.1:p.Arg119=
XM_011524296.2:c.356G=	XP_011522598.1:p.Arg119=
NM_173477.5:c.665G= MANE Select	NP_775748.2:p.Arg222=
NM_001282489.3:c.356G=	NP_001269418.1:p.Arg119=