Canonical Allele Identifier: CA2250000623

Gene: PIGL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16317813C= , CM000679.2:g.16317813C=	GRCh38
NC_000017.10:g.16221127C= , CM000679.1:g.16221127C=	GRCh37
NC_000017.9:g.16161852C=	NCBI36
NG_032651.1:g.105619C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225609.10:c.565C= MANE Select	ENSP00000225609.5:p.Arg189=
ENST00000225609.9:c.565C=	ENSP00000225609.5:p.Arg189=
ENST00000395844.8:c.533C=	ENSP00000379185.3:p.Ala178=
ENST00000477745.5:n.563C=
ENST00000488375.2:n.423C=
ENST00000580201.1:n.545C=
ENST00000581006.5:c.426+17835C=	ENSP00000462432.1:n.426+17835C=
ENST00000596678.2:c.107C=	ENSP00000470064.2:p.Ala36=
ENST00000613719.1:n.987+125C=
NM_004278.3:c.565C=	NP_004269.1:p.Arg189=
XR_243571.2:n.1563C=
XR_429826.2:n.1010C=
XM_017025349.1:c.*729C=	XP_016880838.1:n.*729C=
XM_017025350.1:c.*729C=	XP_016880839.1:n.*729C=
XM_017025351.1:c.*176C=	XP_016880840.1:n.*176C=
XM_017025352.1:c.565C=	XP_016880841.1:p.Arg189=
XM_017025353.1:c.565C=	XP_016880842.1:p.Arg189=
XM_017025354.1:c.533C=	XP_016880843.1:p.Ala178=
XM_017025355.1:c.533C=	XP_016880844.1:p.Ala178=
XM_017025356.1:c.*1042C=	XP_016880845.1:n.*1042C=
NM_004278.4:c.565C= MANE Select	NP_004269.1:p.Arg189=