Canonical Allele Identifier: CA2275255213

Gene: USH1G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74919690G= , CM000679.2:g.74919690G=	GRCh38
NC_000017.10:g.72915785G= , CM000679.1:g.72915785G=	GRCh37
NC_000017.9:g.70427380G=	NCBI36
NG_007882.1:g.8567C=
NG_033062.1:g.416G=
NG_007882.2:g.8574C=
NG_033062.2:g.416G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.1146C= MANE Select	ENSP00000480279.1:p.Asp382=
ENST00000579243.1:c.*745C=	ENSP00000462568.1:n.*745C=
ENST00000614341.4:c.1146C=	ENSP00000480279.1:p.Asp382=
NM_001282489.2:c.837C=	NP_001269418.1:p.Asp279=
NM_173477.4:c.1146C=	NP_775748.2:p.Asp382=
XM_011524296.1:c.837C=	XP_011522598.1:p.Asp279=
XM_011524296.2:c.837C=	XP_011522598.1:p.Asp279=
NM_173477.5:c.1146C= MANE Select	NP_775748.2:p.Asp382=
NM_001282489.3:c.837C=	NP_001269418.1:p.Asp279=