Canonical Allele Identifier: CA2636282124

Gene: PIGL

Linked Data

• gnomAD v4: 17-16317915-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16317915A>G , CM000679.2:g.16317915A>G	GRCh38
NC_000017.10:g.16221229A>G , CM000679.1:g.16221229A>G	GRCh37
NC_000017.9:g.16161954A>G	NCBI36
NG_032651.1:g.105721A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000225609.10:c.660+7A>G MANE Select	ENSP00000225609.5:n.660+7A>G
ENST00000225609.9:c.660+7A>G	ENSP00000225609.5:n.660+7A>G
ENST00000395844.8:c.628+7A>G	ENSP00000379185.3:n.628+7A>G
ENST00000477745.5:n.658+7A>G
ENST00000488375.2:n.518+7A>G
ENST00000581006.5:c.426+17937A>G	ENSP00000462432.1:n.426+17937A>G
ENST00000596678.2:c.202+7A>G	ENSP00000470064.2:n.202+7A>G
ENST00000613719.1:n.987+227A>G
NM_004278.3:c.660+7A>G	NP_004269.1:n.660+7A>G
XR_243571.2:n.1658+7A>G
XM_017025349.1:c.*824+7A>G	XP_016880838.1:n.*824+7A>G
XM_017025350.1:c.*824+7A>G	XP_016880839.1:n.*824+7A>G
XM_017025352.1:c.660+7A>G	XP_016880841.1:n.660+7A>G
XM_017025353.1:c.660+7A>G	XP_016880842.1:n.660+7A>G
XM_017025354.1:c.628+7A>G	XP_016880843.1:n.628+7A>G
XM_017025355.1:c.628+7A>G	XP_016880844.1:n.628+7A>G
XM_017025356.1:c.*1137+7A>G	XP_016880845.1:n.*1137+7A>G
NM_004278.4:c.660+7A>G MANE Select	NP_004269.1:n.660+7A>G