Canonical Allele Identifier: CA2275255365

Gene: USH1G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74919976G= , CM000679.2:g.74919976G=	GRCh38
NC_000017.10:g.72916071G= , CM000679.1:g.72916071G=	GRCh37
NC_000017.9:g.70427666G=	NCBI36
NG_007882.1:g.8281C=
NG_033062.1:g.702G=
NG_007882.2:g.8288C=
NG_033062.2:g.702G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.860C= MANE Select	ENSP00000480279.1:p.Thr287=
ENST00000579243.1:c.*459C=	ENSP00000462568.1:n.*459C=
ENST00000614341.4:c.860C=	ENSP00000480279.1:p.Thr287=
NM_001282489.2:c.551C=	NP_001269418.1:p.Thr184=
NM_173477.4:c.860C=	NP_775748.2:p.Thr287=
XM_011524296.1:c.551C=	XP_011522598.1:p.Thr184=
XM_011524296.2:c.551C=	XP_011522598.1:p.Thr184=
NM_173477.5:c.860C= MANE Select	NP_775748.2:p.Thr287=
NM_001282489.3:c.551C=	NP_001269418.1:p.Thr184=