Canonical Allele Identifier: CA398480343

Gene: PIGL

Linked Data

• MyVariant Identifiers: chr17:g.16221156C>T (hg19) ; chr17:g.16317842C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16317842C>T , CM000679.2:g.16317842C>T	GRCh38
NC_000017.10:g.16221156C>T , CM000679.1:g.16221156C>T	GRCh37
NC_000017.9:g.16161881C>T	NCBI36
NG_032651.1:g.105648C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225609.10:c.594C>T MANE Select	ENSP00000225609.5:p.Pro198=
ENST00000225609.9:c.594C>T	ENSP00000225609.5:p.Pro198=
ENST00000395844.8:c.562C>T	ENSP00000379185.3:p.Leu188Phe
ENST00000477745.5:n.592C>T
ENST00000488375.2:n.452C>T
ENST00000581006.5:c.426+17864C>T	ENSP00000462432.1:n.426+17864C>T
ENST00000596678.2:c.136C>T	ENSP00000470064.2:p.Leu46Phe
ENST00000613719.1:n.987+154C>T
NM_004278.3:c.594C>T	NP_004269.1:p.Pro198=
XR_243571.2:n.1592C>T
XR_429826.2:n.1039C>T
XM_017025349.1:c.*758C>T	XP_016880838.1:n.*758C>T
XM_017025350.1:c.*758C>T	XP_016880839.1:n.*758C>T
XM_017025351.1:c.*205C>T	XP_016880840.1:n.*205C>T
XM_017025352.1:c.594C>T	XP_016880841.1:p.Pro198=
XM_017025353.1:c.594C>T	XP_016880842.1:p.Pro198=
XM_017025354.1:c.562C>T	XP_016880843.1:p.Leu188Phe
XM_017025355.1:c.562C>T	XP_016880844.1:p.Leu188Phe
XM_017025356.1:c.*1071C>T	XP_016880845.1:n.*1071C>T
NM_004278.4:c.594C>T MANE Select	NP_004269.1:p.Pro198=