Canonical Allele Identifier: CA398479413

Gene: PIGL

Linked Data

• MyVariant Identifiers: chr17:g.16203217C>G (hg19) ; chr17:g.16299903C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16299903C>G , CM000679.2:g.16299903C>G	GRCh38
NC_000017.10:g.16203217C>G , CM000679.1:g.16203217C>G	GRCh37
NC_000017.9:g.16143942C>G	NCBI36
NG_032651.1:g.87709C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225609.10:c.351C>G MANE Select	ENSP00000225609.5:p.Asp117Glu
ENST00000225609.9:c.351C>G	ENSP00000225609.5:p.Asp117Glu
ENST00000395844.8:c.351C>G	ENSP00000379185.3:p.Asp117Glu
ENST00000477745.5:n.349C>G
ENST00000498772.6:n.368C>G
ENST00000581006.5:c.351C>G	ENSP00000462432.1:p.Asp117Glu
ENST00000584797.5:c.351C>G	ENSP00000463540.1:p.Asp117Glu
ENST00000585034.5:c.251C>G	ENSP00000464424.1:p.Thr84Ser
ENST00000607144.4:n.387C>G
NM_004278.3:c.351C>G	NP_004269.1:p.Asp117Glu
XM_011524080.1:c.351C>G	XP_011522382.1:p.Asp117Glu
XR_243571.2:n.369C>G
XR_429826.2:n.369C>G
XM_011524080.2:c.351C>G	XP_011522382.1:p.Asp117Glu
XM_017025349.1:c.351C>G	XP_016880838.1:p.Asp117Glu
XM_017025350.1:c.351C>G	XP_016880839.1:p.Asp117Glu
XM_017025351.1:c.351C>G	XP_016880840.1:p.Asp117Glu
XM_017025352.1:c.351C>G	XP_016880841.1:p.Asp117Glu
XM_017025353.1:c.351C>G	XP_016880842.1:p.Asp117Glu
XM_017025354.1:c.351C>G	XP_016880843.1:p.Asp117Glu
XM_017025355.1:c.351C>G	XP_016880844.1:p.Asp117Glu
XM_017025356.1:c.351C>G	XP_016880845.1:p.Asp117Glu
NM_004278.4:c.351C>G MANE Select	NP_004269.1:p.Asp117Glu