Canonical Allele Identifier: CA2250000634

Gene: PIGL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16317814G= , CM000679.2:g.16317814G=	GRCh38
NC_000017.10:g.16221128G= , CM000679.1:g.16221128G=	GRCh37
NC_000017.9:g.16161853G=	NCBI36
NG_032651.1:g.105620G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225609.10:c.566G= MANE Select	ENSP00000225609.5:p.Arg189=
ENST00000225609.9:c.566G=	ENSP00000225609.5:p.Arg189=
ENST00000395844.8:c.534G=	ENSP00000379185.3:p.Ala178=
ENST00000477745.5:n.564G=
ENST00000488375.2:n.424G=
ENST00000580201.1:n.546G=
ENST00000581006.5:c.426+17836G=	ENSP00000462432.1:n.426+17836G=
ENST00000596678.2:c.108G=	ENSP00000470064.2:p.Ala36=
ENST00000613719.1:n.987+126G=
NM_004278.3:c.566G=	NP_004269.1:p.Arg189=
XR_243571.2:n.1564G=
XR_429826.2:n.1011G=
XM_017025349.1:c.*730G=	XP_016880838.1:n.*730G=
XM_017025350.1:c.*730G=	XP_016880839.1:n.*730G=
XM_017025351.1:c.*177G=	XP_016880840.1:n.*177G=
XM_017025352.1:c.566G=	XP_016880841.1:p.Arg189=
XM_017025353.1:c.566G=	XP_016880842.1:p.Arg189=
XM_017025354.1:c.534G=	XP_016880843.1:p.Ala178=
XM_017025355.1:c.534G=	XP_016880844.1:p.Ala178=
XM_017025356.1:c.*1043G=	XP_016880845.1:n.*1043G=
NM_004278.4:c.566G= MANE Select	NP_004269.1:p.Arg189=