Canonical Allele Identifier: CA2249953252
Gene: PIGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16234001A= , CM000679.2:g.16234001A= GRCh38
NC_000017.10:g.16137315A= , CM000679.1:g.16137315A= GRCh37
NC_000017.9:g.16078040A= NCBI36
NG_032651.1:g.21807A=

Transcript Alleles

HGVS Amino-acid change
ENST00000225609.10:c.266A= MANE Select ENSP00000225609.5:p.Lys89=
ENST00000225609.9:c.266A= ENSP00000225609.5:p.Lys89=
ENST00000395844.8:c.266A= ENSP00000379185.3:p.Lys89=
ENST00000470116.2:c.266A= ENSP00000463754.1:p.Lys89=
ENST00000477745.5:n.264A=
ENST00000489009.1:n.256A=
ENST00000498772.6:n.283A=
ENST00000581006.5:c.266A= ENSP00000462432.1:p.Lys89=
ENST00000584797.5:c.266A= ENSP00000463540.1:p.Lys89=
ENST00000585034.5:c.235+16540A= ENSP00000464424.1:n.235+16540A=
ENST00000607144.4:n.302A=
NM_004278.3:c.266A= NP_004269.1:p.Lys89=
XM_011524080.1:c.266A= XP_011522382.1:p.Lys89=
XR_243571.2:n.284A=
XR_429826.2:n.284A=
XM_011524080.2:c.266A= XP_011522382.1:p.Lys89=
XM_017025349.1:c.266A= XP_016880838.1:p.Lys89=
XM_017025350.1:c.266A= XP_016880839.1:p.Lys89=
XM_017025351.1:c.266A= XP_016880840.1:p.Lys89=
XM_017025352.1:c.266A= XP_016880841.1:p.Lys89=
XM_017025353.1:c.266A= XP_016880842.1:p.Lys89=
XM_017025354.1:c.266A= XP_016880843.1:p.Lys89=
XM_017025355.1:c.266A= XP_016880844.1:p.Lys89=
XM_017025356.1:c.266A= XP_016880845.1:p.Lys89=
NM_004278.4:c.266A= MANE Select NP_004269.1:p.Lys89=