Canonical Allele Identifier: CA2275255183

Gene: USH1G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74919630C= , CM000679.2:g.74919630C=	GRCh38
NC_000017.10:g.72915725C= , CM000679.1:g.72915725C=	GRCh37
NC_000017.9:g.70427320C=	NCBI36
NG_007882.1:g.8627G=
NG_033062.1:g.356C=
NG_007882.2:g.8634G=
NG_033062.2:g.356C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.1206G= MANE Select	ENSP00000480279.1:p.Glu402=
ENST00000579243.1:c.*805G=	ENSP00000462568.1:n.*805G=
ENST00000614341.4:c.1206G=	ENSP00000480279.1:p.Glu402=
NM_001282489.2:c.897G=	NP_001269418.1:p.Glu299=
NM_173477.4:c.1206G=	NP_775748.2:p.Glu402=
XM_011524296.1:c.897G=	XP_011522598.1:p.Glu299=
XM_011524296.2:c.897G=	XP_011522598.1:p.Glu299=
NM_173477.5:c.1206G= MANE Select	NP_775748.2:p.Glu402=
NM_001282489.3:c.897G=	NP_001269418.1:p.Glu299=