Canonical Allele Identifier: CA2275255139

Gene: USH1G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74919547C= , CM000679.2:g.74919547C=	GRCh38
NC_000017.10:g.72915642C= , CM000679.1:g.72915642C=	GRCh37
NC_000017.9:g.70427237C=	NCBI36
NG_007882.1:g.8710G=
NG_033062.1:g.273C=
NG_007882.2:g.8717G=
NG_033062.2:g.273C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.1289G= MANE Select	ENSP00000480279.1:p.Ser430=
ENST00000579243.1:c.*888G=	ENSP00000462568.1:n.*888G=
ENST00000614341.4:c.1289G=	ENSP00000480279.1:p.Ser430=
NM_001282489.2:c.980G=	NP_001269418.1:p.Ser327=
NM_173477.4:c.1289G=	NP_775748.2:p.Ser430=
XM_011524296.1:c.980G=	XP_011522598.1:p.Ser327=
XM_011524296.2:c.980G=	XP_011522598.1:p.Ser327=
NM_173477.5:c.1289G= MANE Select	NP_775748.2:p.Ser430=
NM_001282489.3:c.980G=	NP_001269418.1:p.Ser327=