Canonical Allele Identifier: CA2275255169

Gene: USH1G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74919605C= , CM000679.2:g.74919605C=	GRCh38
NC_000017.10:g.72915700C= , CM000679.1:g.72915700C=	GRCh37
NC_000017.9:g.70427295C=	NCBI36
NG_007882.1:g.8652G=
NG_033062.1:g.331C=
NG_007882.2:g.8659G=
NG_033062.2:g.331C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.1231G= MANE Select	ENSP00000480279.1:p.Glu411=
ENST00000579243.1:c.*830G=	ENSP00000462568.1:n.*830G=
ENST00000614341.4:c.1231G=	ENSP00000480279.1:p.Glu411=
NM_001282489.2:c.922G=	NP_001269418.1:p.Glu308=
NM_173477.4:c.1231G=	NP_775748.2:p.Glu411=
XM_011524296.1:c.922G=	XP_011522598.1:p.Glu308=
XM_011524296.2:c.922G=	XP_011522598.1:p.Glu308=
NM_173477.5:c.1231G= MANE Select	NP_775748.2:p.Glu411=
NM_001282489.3:c.922G=	NP_001269418.1:p.Glu308=