Canonical Allele Identifier: CA2361273010
Community Standard Title: NM_080476.5(PIGU):c.926+1469C=
Gene: PIGU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34583968G= , CM000682.2:g.34583968G= GRCh38
NC_000020.10:g.33171772G= , CM000682.1:g.33171772G= GRCh37
NC_000020.9:g.32635433G= NCBI36
NG_011497.1:g.98318C=

Transcript Alleles

HGVS Amino-acid Change
NM_080476.5:c.926+1469C= MANE Select NP_536724.1:n.926+1469C=
ENST00000217446.8:c.926+1469C= MANE Select ENSP00000217446.3:n.926+1469C=
NM_080476.4:c.926+1469C= NP_536724.1:n.926+1469C=
ENST00000217446.7:c.926+1469C= ENSP00000217446.3:n.926+1469C=
ENST00000374820.6:c.866+1469C= ENSP00000363953.2:n.866+1469C=
ENST00000438215.1:c.164+1469C= ENSP00000395755.1:n.164+1469C=
ENST00000480175.1:n.245-2296C=
XM_011528542.1:c.278+1469C= XP_011526844.1:n.278+1469C=
XM_011528542.2:c.278+1469C= XP_011526844.1:n.278+1469C=
XM_017027664.1:c.783-2296C= XP_016883153.1:n.783-2296C=
XR_001754162.1:n.978+1469C=
XR_001754163.1:n.835-2296C=