Canonical Allele Identifier: CA2250000801

Gene: PIGL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16317900C= , CM000679.2:g.16317900C=	GRCh38
NC_000017.10:g.16221214C= , CM000679.1:g.16221214C=	GRCh37
NC_000017.9:g.16161939C=	NCBI36
NG_032651.1:g.105706C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225609.10:c.652C= MANE Select	ENSP00000225609.5:p.Gln218=
ENST00000225609.9:c.652C=	ENSP00000225609.5:p.Gln218=
ENST00000395844.8:c.620C=	ENSP00000379185.3:p.Thr207=
ENST00000477745.5:n.650C=
ENST00000488375.2:n.510C=
ENST00000581006.5:c.426+17922C=	ENSP00000462432.1:n.426+17922C=
ENST00000596678.2:c.194C=	ENSP00000470064.2:p.Thr65=
ENST00000613719.1:n.987+212C=
NM_004278.3:c.652C=	NP_004269.1:p.Gln218=
XR_243571.2:n.1650C=
XM_017025349.1:c.*816C=	XP_016880838.1:n.*816C=
XM_017025350.1:c.*816C=	XP_016880839.1:n.*816C=
XM_017025352.1:c.652C=	XP_016880841.1:p.Gln218=
XM_017025353.1:c.652C=	XP_016880842.1:p.Gln218=
XM_017025354.1:c.620C=	XP_016880843.1:p.Thr207=
XM_017025355.1:c.620C=	XP_016880844.1:p.Thr207=
XM_017025356.1:c.*1129C=	XP_016880845.1:n.*1129C=
NM_004278.4:c.652C= MANE Select	NP_004269.1:p.Gln218=