Canonical Allele Identifier: CA2250000638

Gene: PIGL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16317815C= , CM000679.2:g.16317815C=	GRCh38
NC_000017.10:g.16221129C= , CM000679.1:g.16221129C=	GRCh37
NC_000017.9:g.16161854C=	NCBI36
NG_032651.1:g.105621C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000225609.10:c.567C= MANE Select	ENSP00000225609.5:p.Arg189=
ENST00000225609.9:c.567C=	ENSP00000225609.5:p.Arg189=
ENST00000395844.8:c.535C=	ENSP00000379185.3:p.Gln179=
ENST00000477745.5:n.565C=
ENST00000488375.2:n.425C=
ENST00000580201.1:n.547C=
ENST00000581006.5:c.426+17837C=	ENSP00000462432.1:n.426+17837C=
ENST00000596678.2:c.109C=	ENSP00000470064.2:p.Gln37=
ENST00000613719.1:n.987+127C=
NM_004278.3:c.567C=	NP_004269.1:p.Arg189=
XR_243571.2:n.1565C=
XR_429826.2:n.1012C=
XM_017025349.1:c.*731C=	XP_016880838.1:n.*731C=
XM_017025350.1:c.*731C=	XP_016880839.1:n.*731C=
XM_017025351.1:c.*178C=	XP_016880840.1:n.*178C=
XM_017025352.1:c.567C=	XP_016880841.1:p.Arg189=
XM_017025353.1:c.567C=	XP_016880842.1:p.Arg189=
XM_017025354.1:c.535C=	XP_016880843.1:p.Gln179=
XM_017025355.1:c.535C=	XP_016880844.1:p.Gln179=
XM_017025356.1:c.*1044C=	XP_016880845.1:n.*1044C=
NM_004278.4:c.567C= MANE Select	NP_004269.1:p.Arg189=