Canonical Allele Identifier: CA2250012145

Gene: PIGL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16325870T= , CM000679.2:g.16325870T=	GRCh38
NC_000017.10:g.16229184T= , CM000679.1:g.16229184T=	GRCh37
NC_000017.9:g.16169909T=	NCBI36
NG_032651.1:g.113676T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000225609.10:c.731T= MANE Select	ENSP00000225609.5:p.Met244=
ENST00000225609.9:c.731T=	ENSP00000225609.5:p.Met244=
ENST00000395844.8:c.699T=	ENSP00000379185.3:p.His233=
ENST00000488375.2:n.589T=
ENST00000581006.5:c.427-22822T=	ENSP00000462432.1:n.427-22822T=
ENST00000596678.2:c.273T=	ENSP00000470064.2:p.His91=
ENST00000613719.1:n.987+8182T=
NM_004278.3:c.731T=	NP_004269.1:p.Met244=
XR_243571.2:n.1729T=
XM_017025349.1:c.*895T=	XP_016880838.1:n.*895T=
XM_017025350.1:c.*895T=	XP_016880839.1:n.*895T=
XM_017025352.1:c.731T=	XP_016880841.1:p.Met244=
XM_017025353.1:c.731T=	XP_016880842.1:p.Met244=
XM_017025354.1:c.699T=	XP_016880843.1:p.His233=
XM_017025355.1:c.699T=	XP_016880844.1:p.His233=
XM_017025356.1:c.*1208T=	XP_016880845.1:n.*1208T=
NM_004278.4:c.731T= MANE Select	NP_004269.1:p.Met244=