Canonical Allele Identifier: CA2250012125

Gene: PIGL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16325865G= , CM000679.2:g.16325865G=	GRCh38
NC_000017.10:g.16229179G= , CM000679.1:g.16229179G=	GRCh37
NC_000017.9:g.16169904G=	NCBI36
NG_032651.1:g.113671G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000225609.10:c.726G= MANE Select	ENSP00000225609.5:p.Arg242=
ENST00000225609.9:c.726G=	ENSP00000225609.5:p.Arg242=
ENST00000395844.8:c.694G=	ENSP00000379185.3:p.Val232=
ENST00000488375.2:n.584G=
ENST00000581006.5:c.427-22827G=	ENSP00000462432.1:n.427-22827G=
ENST00000596678.2:c.268G=	ENSP00000470064.2:p.Val90=
ENST00000613719.1:n.987+8177G=
NM_004278.3:c.726G=	NP_004269.1:p.Arg242=
XR_243571.2:n.1724G=
XM_017025349.1:c.*890G=	XP_016880838.1:n.*890G=
XM_017025350.1:c.*890G=	XP_016880839.1:n.*890G=
XM_017025352.1:c.726G=	XP_016880841.1:p.Arg242=
XM_017025353.1:c.726G=	XP_016880842.1:p.Arg242=
XM_017025354.1:c.694G=	XP_016880843.1:p.Val232=
XM_017025355.1:c.694G=	XP_016880844.1:p.Val232=
XM_017025356.1:c.*1203G=	XP_016880845.1:n.*1203G=
NM_004278.4:c.726G= MANE Select	NP_004269.1:p.Arg242=