Canonical Allele Identifier: CA398481024

Gene: PIGL

Linked Data

• MyVariant Identifiers: chr17:g.16229178G>T (hg19) ; chr17:g.16325864G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16325864G>T , CM000679.2:g.16325864G>T	GRCh38
NC_000017.10:g.16229178G>T , CM000679.1:g.16229178G>T	GRCh37
NC_000017.9:g.16169903G>T	NCBI36
NG_032651.1:g.113670G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000225609.10:c.725G>T MANE Select	ENSP00000225609.5:p.Arg242Leu
ENST00000225609.9:c.725G>T	ENSP00000225609.5:p.Arg242Leu
ENST00000395844.8:c.693G>T	ENSP00000379185.3:p.Pro231=
ENST00000488375.2:n.583G>T
ENST00000581006.5:c.427-22828G>T	ENSP00000462432.1:n.427-22828G>T
ENST00000596678.2:c.267G>T	ENSP00000470064.2:p.Pro89=
ENST00000613719.1:n.987+8176G>T
NM_004278.3:c.725G>T	NP_004269.1:p.Arg242Leu
XR_243571.2:n.1723G>T
XM_017025349.1:c.*889G>T	XP_016880838.1:n.*889G>T
XM_017025350.1:c.*889G>T	XP_016880839.1:n.*889G>T
XM_017025352.1:c.725G>T	XP_016880841.1:p.Arg242Leu
XM_017025353.1:c.725G>T	XP_016880842.1:p.Arg242Leu
XM_017025354.1:c.693G>T	XP_016880843.1:p.Pro231=
XM_017025355.1:c.693G>T	XP_016880844.1:p.Pro231=
XM_017025356.1:c.*1202G>T	XP_016880845.1:n.*1202G>T
NM_004278.4:c.725G>T MANE Select	NP_004269.1:p.Arg242Leu