Canonical Allele Identifier: CA16620341
Gene: WDR81 HGNC NCBI

Linked Data

ClinVar Variation Id: 423034
ClinVar RCV Id: RCV000478085
dbSNP Id: rs1064796183

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1728516del , CM000679.2:g.1728516del GRCh38
NC_000017.10:g.1631810del , CM000679.1:g.1631810del GRCh37
NC_000017.9:g.1578560del NCBI36
NG_032811.1:g.16994del

Transcript Alleles

HGVS Amino-acid change
ENST00000409644.6:c.3557del MANE Select ENSP00000386609.1:p.Thr1186ArgfsTer?
ENST00000309182.9:c.404del ENSP00000312074.5:p.Thr135ArgfsTer?
ENST00000409644.5:c.3557del ENSP00000386609.1:p.Thr1186ArgfsTer?
ENST00000418841.5:c.-89+3730del ENSP00000395198.1:n.-89+3730del
ENST00000419248.5:c.-14-1864del ENSP00000407845.1:n.-14-1864del
ENST00000437219.6:c.59-1864del ENSP00000391074.2:n.59-1864del
ENST00000446363.5:c.-308-2239del ENSP00000401560.1:n.-308-2239del
ENST00000455636.5:c.59-1864del ENSP00000395226.1:n.59-1864del
ENST00000464528.5:n.943del
ENST00000468539.5:c.63-3809del ENSP00000460742.1:n.63-3809del
ENST00000492901.1:n.88-1864del
ENST00000575206.1:c.307del
NM_001163673.1:c.59-1864del NP_001157145.1:n.59-1864del
NM_001163809.1:c.3557del NP_001157281.1:p.Thr1186ArgfsTer?
NM_001163811.1:c.-14-1864del NP_001157283.1:n.-14-1864del
NM_152348.3:c.404del NP_689561.2:p.Thr135ArgfsTer?
XM_005256454.2:c.3557del XP_005256511.1:p.Thr1186ArgfsTer?
XM_011523650.1:c.3557del XP_011521952.1:p.Thr1186ArgfsTer?
XM_011523651.1:c.404del XP_011521953.1:p.Thr135ArgfsTer?
XR_933973.1:n.3701del
XM_011523651.2:c.404del XP_011521953.1:p.Thr135ArgfsTer?
XM_017024184.1:c.3557del XP_016879673.1:p.Thr1186ArgfsTer?
XR_001752427.1:n.3709del
XR_933973.2:n.3709del
NM_001163809.2:c.3557del MANE Select NP_001157281.1:p.Thr1186ArgfsTer?
NM_001163811.2:c.-14-1864del NP_001157283.1:n.-14-1864del
NM_152348.4:c.404del NP_689561.2:p.Thr135ArgfsTer?
NM_001163673.2:c.59-1864del NP_001157145.1:n.59-1864del