Canonical Allele Identifier: CA2275255436

Gene: USH1G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74920105A= , CM000679.2:g.74920105A=	GRCh38
NC_000017.10:g.72916200A= , CM000679.1:g.72916200A=	GRCh37
NC_000017.9:g.70427795A=	NCBI36
NG_007882.1:g.8152T=
NG_033062.1:g.831A=
NG_007882.2:g.8159T=
NG_033062.2:g.831A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.731T= MANE Select	ENSP00000480279.1:p.Leu244=
ENST00000579243.1:c.*330T=	ENSP00000462568.1:n.*330T=
ENST00000614341.4:c.731T=	ENSP00000480279.1:p.Leu244=
NM_001282489.2:c.422T=	NP_001269418.1:p.Leu141=
NM_173477.4:c.731T=	NP_775748.2:p.Leu244=
XM_011524296.1:c.422T=	XP_011522598.1:p.Leu141=
XM_011524296.2:c.422T=	XP_011522598.1:p.Leu141=
NM_173477.5:c.731T= MANE Select	NP_775748.2:p.Leu244=
NM_001282489.3:c.422T=	NP_001269418.1:p.Leu141=