Canonical Allele Identifier: CA2249995872
Gene: PIGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16313567G= , CM000679.2:g.16313567G= GRCh38
NC_000017.10:g.16216881G= , CM000679.1:g.16216881G= GRCh37
NC_000017.9:g.16157606G= NCBI36
NG_032651.1:g.101373G=

Transcript Alleles

HGVS Amino-acid change
ENST00000225609.10:c.447G= MANE Select ENSP00000225609.5:p.Gly149=
ENST00000225609.9:c.447G= ENSP00000225609.5:p.Gly149=
ENST00000395844.8:c.447G= ENSP00000379185.3:p.Gly149=
ENST00000477745.5:n.445G=
ENST00000498772.6:n.464G=
ENST00000580201.1:n.459G=
ENST00000581006.5:c.426+13589G= ENSP00000462432.1:n.426+13589G=
ENST00000584797.5:c.447G= ENSP00000463540.1:p.Gly149=
ENST00000585034.5:c.*41G= ENSP00000464424.1:n.*41G=
ENST00000596678.2:c.21G= ENSP00000470064.2:p.Gly7=
NM_004278.3:c.447G= NP_004269.1:p.Gly149=
XM_011524080.1:c.447G= XP_011522382.1:p.Gly149=
XR_243571.2:n.465G=
XR_429826.2:n.465G=
XM_011524080.2:c.447G= XP_011522382.1:p.Gly149=
XM_017025349.1:c.447G= XP_016880838.1:p.Gly149=
XM_017025350.1:c.447G= XP_016880839.1:p.Gly149=
XM_017025351.1:c.447G= XP_016880840.1:p.Gly149=
XM_017025352.1:c.447G= XP_016880841.1:p.Gly149=
XM_017025353.1:c.447G= XP_016880842.1:p.Gly149=
XM_017025354.1:c.447G= XP_016880843.1:p.Gly149=
XM_017025355.1:c.447G= XP_016880844.1:p.Gly149=
XM_017025356.1:c.447G= XP_016880845.1:p.Gly149=
NM_004278.4:c.447G= MANE Select NP_004269.1:p.Gly149=