Canonical Allele Identifier: CA2808611473
Gene: PIGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16317933_16317934insA , CM000679.2:g.16317933_16317934insA GRCh38
NC_000017.10:g.16221247_16221248insA , CM000679.1:g.16221247_16221248insA GRCh37
NC_000017.9:g.16161972_16161973insA NCBI36
NG_032651.1:g.105739_105740insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000225609.10:c.660+25_660+26insA MANE Select ENSP00000225609.5:n.660+25_660+26insA
ENST00000225609.9:c.660+25_660+26insA ENSP00000225609.5:n.660+25_660+26insA
ENST00000395844.8:c.628+25_628+26insA ENSP00000379185.3:n.628+25_628+26insA
ENST00000477745.5:n.658+25_658+26insA
ENST00000488375.2:n.518+25_518+26insA
ENST00000581006.5:c.426+17955_426+17956insA ENSP00000462432.1:n.426+17955_426+17956insA
ENST00000596678.2:c.202+25_202+26insA ENSP00000470064.2:n.202+25_202+26insA
ENST00000613719.1:n.987+245_987+246insA
NM_004278.3:c.660+25_660+26insA NP_004269.1:n.660+25_660+26insA
XR_243571.2:n.1658+25_1658+26insA
XM_017025349.1:c.*824+25_*824+26insA XP_016880838.1:n.*824+25_*824+26insA
XM_017025350.1:c.*824+25_*824+26insA XP_016880839.1:n.*824+25_*824+26insA
XM_017025352.1:c.660+25_660+26insA XP_016880841.1:n.660+25_660+26insA
XM_017025353.1:c.660+25_660+26insA XP_016880842.1:n.660+25_660+26insA
XM_017025354.1:c.628+25_628+26insA XP_016880843.1:n.628+25_628+26insA
XM_017025355.1:c.628+25_628+26insA XP_016880844.1:n.628+25_628+26insA
XM_017025356.1:c.*1137+25_*1137+26insA XP_016880845.1:n.*1137+25_*1137+26insA
NM_004278.4:c.660+25_660+26insA MANE Select NP_004269.1:n.660+25_660+26insA