Canonical Allele Identifier: CA2250000811

Gene: PIGL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16317901A= , CM000679.2:g.16317901A=	GRCh38
NC_000017.10:g.16221215A= , CM000679.1:g.16221215A=	GRCh37
NC_000017.9:g.16161940A=	NCBI36
NG_032651.1:g.105707A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225609.10:c.653A= MANE Select	ENSP00000225609.5:p.Gln218=
ENST00000225609.9:c.653A=	ENSP00000225609.5:p.Gln218=
ENST00000395844.8:c.621A=	ENSP00000379185.3:p.Thr207=
ENST00000477745.5:n.651A=
ENST00000488375.2:n.511A=
ENST00000581006.5:c.426+17923A=	ENSP00000462432.1:n.426+17923A=
ENST00000596678.2:c.195A=	ENSP00000470064.2:p.Thr65=
ENST00000613719.1:n.987+213A=
NM_004278.3:c.653A=	NP_004269.1:p.Gln218=
XR_243571.2:n.1651A=
XM_017025349.1:c.*817A=	XP_016880838.1:n.*817A=
XM_017025350.1:c.*817A=	XP_016880839.1:n.*817A=
XM_017025352.1:c.653A=	XP_016880841.1:p.Gln218=
XM_017025353.1:c.653A=	XP_016880842.1:p.Gln218=
XM_017025354.1:c.621A=	XP_016880843.1:p.Thr207=
XM_017025355.1:c.621A=	XP_016880844.1:p.Thr207=
XM_017025356.1:c.*1130A=	XP_016880845.1:n.*1130A=
NM_004278.4:c.653A= MANE Select	NP_004269.1:p.Gln218=