Canonical Allele Identifier: CA2250001093

Gene: PIGL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16318069C= , CM000679.2:g.16318069C=	GRCh38
NC_000017.10:g.16221383C= , CM000679.1:g.16221383C=	GRCh37
NC_000017.9:g.16162108C=	NCBI36
NG_032651.1:g.105875C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225609.10:c.660+161C= MANE Select	ENSP00000225609.5:n.660+161C=
ENST00000225609.9:c.660+161C=	ENSP00000225609.5:n.660+161C=
ENST00000395844.8:c.628+161C=	ENSP00000379185.3:n.628+161C=
ENST00000477745.5:n.658+161C=
ENST00000488375.2:n.518+161C=
ENST00000581006.5:c.426+18091C=	ENSP00000462432.1:n.426+18091C=
ENST00000596678.2:c.202+161C=	ENSP00000470064.2:n.202+161C=
ENST00000613719.1:n.987+381C=
NM_004278.3:c.660+161C=	NP_004269.1:n.660+161C=
XR_243571.2:n.1658+161C=
XM_017025349.1:c.*824+161C=	XP_016880838.1:n.*824+161C=
XM_017025350.1:c.*824+161C=	XP_016880839.1:n.*824+161C=
XM_017025352.1:c.660+161C=	XP_016880841.1:n.660+161C=
XM_017025353.1:c.660+161C=	XP_016880842.1:n.660+161C=
XM_017025354.1:c.628+161C=	XP_016880843.1:n.628+161C=
XM_017025355.1:c.628+161C=	XP_016880844.1:n.628+161C=
XM_017025356.1:c.*1137+161C=	XP_016880845.1:n.*1137+161C=
NM_004278.4:c.660+161C= MANE Select	NP_004269.1:n.660+161C=