Canonical Allele Identifier: CA2576218723
Gene: PIGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16313484_16313485del , CM000679.2:g.16313484_16313485del GRCh38
NC_000017.10:g.16216798_16216799del , CM000679.1:g.16216798_16216799del GRCh37
NC_000017.9:g.16157523_16157524del NCBI36
NG_032651.1:g.101290_101291del

Transcript Alleles

HGVS Amino-acid change
ENST00000225609.10:c.427-63_427-62del MANE Select ENSP00000225609.5:n.427-63_427-62del
ENST00000225609.9:c.427-63_427-62del ENSP00000225609.5:n.427-63_427-62del
ENST00000395844.8:c.427-63_427-62del ENSP00000379185.3:n.427-63_427-62del
ENST00000477745.5:n.425-63_425-62del
ENST00000498772.6:n.444-63_444-62del
ENST00000580201.1:n.439-63_439-62del
ENST00000581006.5:c.426+13506_426+13507del ENSP00000462432.1:n.426+13506_426+13507del
ENST00000584797.5:c.427-63_427-62del ENSP00000463540.1:n.427-63_427-62del
ENST00000585034.5:c.*21-63_*21-62del ENSP00000464424.1:n.*21-63_*21-62del
NM_004278.3:c.427-63_427-62del NP_004269.1:n.427-63_427-62del
XM_011524080.1:c.427-63_427-62del XP_011522382.1:n.427-63_427-62del
XR_243571.2:n.445-63_445-62del
XR_429826.2:n.445-63_445-62del
XM_011524080.2:c.427-63_427-62del XP_011522382.1:n.427-63_427-62del
XM_017025349.1:c.427-63_427-62del XP_016880838.1:n.427-63_427-62del
XM_017025350.1:c.427-63_427-62del XP_016880839.1:n.427-63_427-62del
XM_017025351.1:c.427-63_427-62del XP_016880840.1:n.427-63_427-62del
XM_017025352.1:c.427-63_427-62del XP_016880841.1:n.427-63_427-62del
XM_017025353.1:c.427-63_427-62del XP_016880842.1:n.427-63_427-62del
XM_017025354.1:c.427-63_427-62del XP_016880843.1:n.427-63_427-62del
XM_017025355.1:c.427-63_427-62del XP_016880844.1:n.427-63_427-62del
XM_017025356.1:c.427-63_427-62del XP_016880845.1:n.427-63_427-62del
NM_004278.4:c.427-63_427-62del MANE Select NP_004269.1:n.427-63_427-62del