Canonical Allele Identifier: CA398480456

Gene: PIGL

Linked Data

• gnomAD v4: 17-16317885-A-C
• MyVariant Identifiers: chr17:g.16221199A>C (hg19) ; chr17:g.16317885A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16317885A>C , CM000679.2:g.16317885A>C	GRCh38
NC_000017.10:g.16221199A>C , CM000679.1:g.16221199A>C	GRCh37
NC_000017.9:g.16161924A>C	NCBI36
NG_032651.1:g.105691A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225609.10:c.637A>C MANE Select	ENSP00000225609.5:p.Ser213Arg
ENST00000225609.9:c.637A>C	ENSP00000225609.5:p.Ser213Arg
ENST00000395844.8:c.605A>C	ENSP00000379185.3:p.Gln202Pro
ENST00000477745.5:n.635A>C
ENST00000488375.2:n.495A>C
ENST00000581006.5:c.426+17907A>C	ENSP00000462432.1:n.426+17907A>C
ENST00000596678.2:c.179A>C	ENSP00000470064.2:p.Gln60Pro
ENST00000613719.1:n.987+197A>C
NM_004278.3:c.637A>C	NP_004269.1:p.Ser213Arg
XR_243571.2:n.1635A>C
XM_017025349.1:c.*801A>C	XP_016880838.1:n.*801A>C
XM_017025350.1:c.*801A>C	XP_016880839.1:n.*801A>C
XM_017025352.1:c.637A>C	XP_016880841.1:p.Ser213Arg
XM_017025353.1:c.637A>C	XP_016880842.1:p.Ser213Arg
XM_017025354.1:c.605A>C	XP_016880843.1:p.Gln202Pro
XM_017025355.1:c.605A>C	XP_016880844.1:p.Gln202Pro
XM_017025356.1:c.*1114A>C	XP_016880845.1:n.*1114A>C
NM_004278.4:c.637A>C MANE Select	NP_004269.1:p.Ser213Arg