Canonical Allele Identifier: CA398480282

Gene: PIGL

Linked Data

• COSMIC: COSM4064176
• MyVariant Identifiers: chr17:g.16221134A>G (hg19) ; chr17:g.16317820A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16317820A>G , CM000679.2:g.16317820A>G	GRCh38
NC_000017.10:g.16221134A>G , CM000679.1:g.16221134A>G	GRCh37
NC_000017.9:g.16161859A>G	NCBI36
NG_032651.1:g.105626A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225609.10:c.572A>G MANE Select	ENSP00000225609.5:p.Tyr191Cys
ENST00000225609.9:c.572A>G	ENSP00000225609.5:p.Tyr191Cys
ENST00000395844.8:c.540A>G	ENSP00000379185.3:p.Val180=
ENST00000477745.5:n.570A>G
ENST00000488375.2:n.430A>G
ENST00000581006.5:c.426+17842A>G	ENSP00000462432.1:n.426+17842A>G
ENST00000596678.2:c.114A>G	ENSP00000470064.2:p.Val38=
ENST00000613719.1:n.987+132A>G
NM_004278.3:c.572A>G	NP_004269.1:p.Tyr191Cys
XR_243571.2:n.1570A>G
XR_429826.2:n.1017A>G
XM_017025349.1:c.*736A>G	XP_016880838.1:n.*736A>G
XM_017025350.1:c.*736A>G	XP_016880839.1:n.*736A>G
XM_017025351.1:c.*183A>G	XP_016880840.1:n.*183A>G
XM_017025352.1:c.572A>G	XP_016880841.1:p.Tyr191Cys
XM_017025353.1:c.572A>G	XP_016880842.1:p.Tyr191Cys
XM_017025354.1:c.540A>G	XP_016880843.1:p.Val180=
XM_017025355.1:c.540A>G	XP_016880844.1:p.Val180=
XM_017025356.1:c.*1049A>G	XP_016880845.1:n.*1049A>G
NM_004278.4:c.572A>G MANE Select	NP_004269.1:p.Tyr191Cys