Canonical Allele Identifier: CA2250012113

Gene: PIGL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16325863C= , CM000679.2:g.16325863C=	GRCh38
NC_000017.10:g.16229177C= , CM000679.1:g.16229177C=	GRCh37
NC_000017.9:g.16169902C=	NCBI36
NG_032651.1:g.113669C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000225609.10:c.724C= MANE Select	ENSP00000225609.5:p.Arg242=
ENST00000225609.9:c.724C=	ENSP00000225609.5:p.Arg242=
ENST00000395844.8:c.692C=	ENSP00000379185.3:p.Pro231=
ENST00000488375.2:n.582C=
ENST00000581006.5:c.427-22829C=	ENSP00000462432.1:n.427-22829C=
ENST00000596678.2:c.266C=	ENSP00000470064.2:p.Pro89=
ENST00000613719.1:n.987+8175C=
NM_004278.3:c.724C=	NP_004269.1:p.Arg242=
XR_243571.2:n.1722C=
XM_017025349.1:c.*888C=	XP_016880838.1:n.*888C=
XM_017025350.1:c.*888C=	XP_016880839.1:n.*888C=
XM_017025352.1:c.724C=	XP_016880841.1:p.Arg242=
XM_017025353.1:c.724C=	XP_016880842.1:p.Arg242=
XM_017025354.1:c.692C=	XP_016880843.1:p.Pro231=
XM_017025355.1:c.692C=	XP_016880844.1:p.Pro231=
XM_017025356.1:c.*1201C=	XP_016880845.1:n.*1201C=
NM_004278.4:c.724C= MANE Select	NP_004269.1:p.Arg242=