Canonical Allele Identifier: CA2249999017
Gene: PIGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16316744A= , CM000679.2:g.16316744A= GRCh38
NC_000017.10:g.16220058A= , CM000679.1:g.16220058A= GRCh37
NC_000017.9:g.16160783A= NCBI36
NG_032651.1:g.104550A=

Transcript Alleles

HGVS Amino-acid change
ENST00000225609.10:c.526+32A= MANE Select ENSP00000225609.5:n.526+32A=
ENST00000225609.9:c.526+32A= ENSP00000225609.5:n.526+32A=
ENST00000395844.8:c.495-1031A= ENSP00000379185.3:n.495-1031A=
ENST00000477745.5:n.524+32A=
ENST00000498772.6:n.575A=
ENST00000580201.1:n.507-1031A=
ENST00000581006.5:c.426+16766A= ENSP00000462432.1:n.426+16766A=
ENST00000584797.5:c.526+32A= ENSP00000463540.1:n.526+32A=
ENST00000585034.5:c.*152A= ENSP00000464424.1:n.*152A=
ENST00000596678.2:c.69-1031A= ENSP00000470064.2:n.69-1031A=
ENST00000613719.1:n.43A=
NM_004278.3:c.526+32A= NP_004269.1:n.526+32A=
XR_243571.2:n.544+32A=
XR_429826.2:n.544+32A=
XM_017025349.1:c.526+32A= XP_016880838.1:n.526+32A=
XM_017025350.1:c.526+32A= XP_016880839.1:n.526+32A=
XM_017025351.1:c.526+32A= XP_016880840.1:n.526+32A=
XM_017025352.1:c.526+32A= XP_016880841.1:n.526+32A=
XM_017025353.1:c.526+32A= XP_016880842.1:n.526+32A=
XM_017025354.1:c.495-1031A= XP_016880843.1:n.495-1031A=
XM_017025355.1:c.495-1031A= XP_016880844.1:n.495-1031A=
XM_017025356.1:c.558A= XP_016880845.1:p.Gln186=
NM_004278.4:c.526+32A= MANE Select NP_004269.1:n.526+32A=