Canonical Allele Identifier: CA498043107

Gene: PIGL

Linked Data

• MyVariant Identifiers: chr17:g.16216878A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16313564A>G , CM000679.2:g.16313564A>G	GRCh38
NC_000017.10:g.16216878A>G , CM000679.1:g.16216878A>G	GRCh37
NC_000017.9:g.16157603A>G	NCBI36
NG_032651.1:g.101370A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000225609.10:c.444A>G MANE Select	ENSP00000225609.5:p.Ala148=
ENST00000225609.9:c.444A>G	ENSP00000225609.5:p.Ala148=
ENST00000395844.8:c.444A>G	ENSP00000379185.3:p.Ala148=
ENST00000477745.5:n.442A>G
ENST00000498772.6:n.461A>G
ENST00000580201.1:n.456A>G
ENST00000581006.5:c.426+13586A>G	ENSP00000462432.1:n.426+13586A>G
ENST00000584797.5:c.444A>G	ENSP00000463540.1:p.Ala148=
ENST00000585034.5:c.*38A>G	ENSP00000464424.1:n.*38A>G
ENST00000596678.2:c.18A>G	ENSP00000470064.2:p.Ala6=
NM_004278.3:c.444A>G	NP_004269.1:p.Ala148=
XM_011524080.1:c.444A>G	XP_011522382.1:p.Ala148=
XR_243571.2:n.462A>G
XR_429826.2:n.462A>G
XM_011524080.2:c.444A>G	XP_011522382.1:p.Ala148=
XM_017025349.1:c.444A>G	XP_016880838.1:p.Ala148=
XM_017025350.1:c.444A>G	XP_016880839.1:p.Ala148=
XM_017025351.1:c.444A>G	XP_016880840.1:p.Ala148=
XM_017025352.1:c.444A>G	XP_016880841.1:p.Ala148=
XM_017025353.1:c.444A>G	XP_016880842.1:p.Ala148=
XM_017025354.1:c.444A>G	XP_016880843.1:p.Ala148=
XM_017025355.1:c.444A>G	XP_016880844.1:p.Ala148=
XM_017025356.1:c.444A>G	XP_016880845.1:p.Ala148=
NM_004278.4:c.444A>G MANE Select	NP_004269.1:p.Ala148=