Canonical Allele Identifier: CA498042663

Gene: PIGL

Linked Data

• MyVariant Identifiers: chr17:g.16203214T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16299900T>C , CM000679.2:g.16299900T>C	GRCh38
NC_000017.10:g.16203214T>C , CM000679.1:g.16203214T>C	GRCh37
NC_000017.9:g.16143939T>C	NCBI36
NG_032651.1:g.87706T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225609.10:c.348T>C MANE Select	ENSP00000225609.5:p.Asp116=
ENST00000225609.9:c.348T>C	ENSP00000225609.5:p.Asp116=
ENST00000395844.8:c.348T>C	ENSP00000379185.3:p.Asp116=
ENST00000477745.5:n.346T>C
ENST00000498772.6:n.365T>C
ENST00000581006.5:c.348T>C	ENSP00000462432.1:p.Asp116=
ENST00000584797.5:c.348T>C	ENSP00000463540.1:p.Asp116=
ENST00000585034.5:c.248T>C	ENSP00000464424.1:p.Met83Thr
ENST00000607144.4:n.384T>C
NM_004278.3:c.348T>C	NP_004269.1:p.Asp116=
XM_011524080.1:c.348T>C	XP_011522382.1:p.Asp116=
XR_243571.2:n.366T>C
XR_429826.2:n.366T>C
XM_011524080.2:c.348T>C	XP_011522382.1:p.Asp116=
XM_017025349.1:c.348T>C	XP_016880838.1:p.Asp116=
XM_017025350.1:c.348T>C	XP_016880839.1:p.Asp116=
XM_017025351.1:c.348T>C	XP_016880840.1:p.Asp116=
XM_017025352.1:c.348T>C	XP_016880841.1:p.Asp116=
XM_017025353.1:c.348T>C	XP_016880842.1:p.Asp116=
XM_017025354.1:c.348T>C	XP_016880843.1:p.Asp116=
XM_017025355.1:c.348T>C	XP_016880844.1:p.Asp116=
XM_017025356.1:c.348T>C	XP_016880845.1:p.Asp116=
NM_004278.4:c.348T>C MANE Select	NP_004269.1:p.Asp116=