Canonical Allele Identifier: CA2250000915
Gene: PIGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16317954_16317955delinsCA , CM000679.2:g.16317954_16317955delinsCA GRCh38
NC_000017.10:g.16221268_16221269delinsCA , CM000679.1:g.16221268_16221269delinsCA GRCh37
NC_000017.9:g.16161993_16161994delinsCA NCBI36
NG_032651.1:g.105760_105761delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000225609.10:c.660+46_660+47delinsCA MANE Select ENSP00000225609.5:n.660+46_660+47delinsCA
ENST00000225609.9:c.660+46_660+47delinsCA ENSP00000225609.5:n.660+46_660+47delinsCA
ENST00000395844.8:c.628+46_628+47delinsCA ENSP00000379185.3:n.628+46_628+47delinsCA
ENST00000477745.5:n.658+46_658+47delinsCA
ENST00000488375.2:n.518+46_518+47delinsCA
ENST00000581006.5:c.426+17976_426+17977delinsCA ENSP00000462432.1:n.426+17976_426+17977delinsCA
ENST00000596678.2:c.202+46_202+47delinsCA ENSP00000470064.2:n.202+46_202+47delinsCA
ENST00000613719.1:n.987+266_987+267delinsCA
NM_004278.3:c.660+46_660+47delinsCA NP_004269.1:n.660+46_660+47delinsCA
XR_243571.2:n.1658+46_1658+47delinsCA
XM_017025349.1:c.*824+46_*824+47delinsCA XP_016880838.1:n.*824+46_*824+47delinsCA
XM_017025350.1:c.*824+46_*824+47delinsCA XP_016880839.1:n.*824+46_*824+47delinsCA
XM_017025352.1:c.660+46_660+47delinsCA XP_016880841.1:n.660+46_660+47delinsCA
XM_017025353.1:c.660+46_660+47delinsCA XP_016880842.1:n.660+46_660+47delinsCA
XM_017025354.1:c.628+46_628+47delinsCA XP_016880843.1:n.628+46_628+47delinsCA
XM_017025355.1:c.628+46_628+47delinsCA XP_016880844.1:n.628+46_628+47delinsCA
XM_017025356.1:c.*1137+46_*1137+47delinsCA XP_016880845.1:n.*1137+46_*1137+47delinsCA
NM_004278.4:c.660+46_660+47delinsCA MANE Select NP_004269.1:n.660+46_660+47delinsCA