Canonical Allele Identifier: CA2249995873
Gene: PIGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16313568G= , CM000679.2:g.16313568G= GRCh38
NC_000017.10:g.16216882G= , CM000679.1:g.16216882G= GRCh37
NC_000017.9:g.16157607G= NCBI36
NG_032651.1:g.101374G=

Transcript Alleles

HGVS Amino-acid change
ENST00000225609.10:c.448G= MANE Select ENSP00000225609.5:p.Gly150=
ENST00000225609.9:c.448G= ENSP00000225609.5:p.Gly150=
ENST00000395844.8:c.448G= ENSP00000379185.3:p.Gly150=
ENST00000477745.5:n.446G=
ENST00000498772.6:n.465G=
ENST00000580201.1:n.460G=
ENST00000581006.5:c.426+13590G= ENSP00000462432.1:n.426+13590G=
ENST00000584797.5:c.448G= ENSP00000463540.1:p.Gly150=
ENST00000585034.5:c.*42G= ENSP00000464424.1:n.*42G=
ENST00000596678.2:c.22G= ENSP00000470064.2:p.Gly8=
NM_004278.3:c.448G= NP_004269.1:p.Gly150=
XM_011524080.1:c.448G= XP_011522382.1:p.Gly150=
XR_243571.2:n.466G=
XR_429826.2:n.466G=
XM_011524080.2:c.448G= XP_011522382.1:p.Gly150=
XM_017025349.1:c.448G= XP_016880838.1:p.Gly150=
XM_017025350.1:c.448G= XP_016880839.1:p.Gly150=
XM_017025351.1:c.448G= XP_016880840.1:p.Gly150=
XM_017025352.1:c.448G= XP_016880841.1:p.Gly150=
XM_017025353.1:c.448G= XP_016880842.1:p.Gly150=
XM_017025354.1:c.448G= XP_016880843.1:p.Gly150=
XM_017025355.1:c.448G= XP_016880844.1:p.Gly150=
XM_017025356.1:c.448G= XP_016880845.1:p.Gly150=
NM_004278.4:c.448G= MANE Select NP_004269.1:p.Gly150=