Canonical Allele Identifier: CA980696881
Gene: WDR81 HGNC NCBI

Linked Data

dbSNP Id: rs1915430227

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1728215del , CM000679.2:g.1728215del GRCh38
NC_000017.10:g.1631509del , CM000679.1:g.1631509del GRCh37
NC_000017.9:g.1578259del NCBI36
NG_032811.1:g.16693del

Transcript Alleles

HGVS Amino-acid Change
ENST00000409644.6:c.3256del MANE Select ENSP00000386609.1:p.Gln1086LysfsTer6
ENST00000309182.9:c.103del ENSP00000312074.5:p.Gln35LysfsTer6
ENST00000409644.5:c.3256del ENSP00000386609.1:p.Gln1086LysfsTer6
ENST00000418841.5:c.-89+3429del ENSP00000395198.1:n.-89+3429del
ENST00000419248.5:c.-14-2165del ENSP00000407845.1:n.-14-2165del
ENST00000437219.6:c.59-2165del ENSP00000391074.2:n.59-2165del
ENST00000446363.5:c.-308-2540del ENSP00000401560.1:n.-308-2540del
ENST00000455636.5:c.59-2165del ENSP00000395226.1:n.59-2165del
ENST00000464528.5:n.642del
ENST00000468539.5:c.63-4110del ENSP00000460742.1:n.63-4110del
ENST00000492901.1:n.88-2165del
ENST00000575206.1:c.6del
NM_001163673.1:c.59-2165del NP_001157145.1:n.59-2165del
NM_001163809.1:c.3256del NP_001157281.1:p.Gln1086LysfsTer6
NM_001163811.1:c.-14-2165del NP_001157283.1:n.-14-2165del
NM_152348.3:c.103del NP_689561.2:p.Gln35LysfsTer6
XM_005256454.2:c.3256del XP_005256511.1:p.Gln1086LysfsTer6
XM_011523650.1:c.3256del XP_011521952.1:p.Gln1086LysfsTer6
XM_011523651.1:c.103del XP_011521953.1:p.Gln35LysfsTer6
XR_933973.1:n.3400del
XM_011523651.2:c.103del XP_011521953.1:p.Gln35LysfsTer6
XM_017024184.1:c.3256del XP_016879673.1:p.Gln1086LysfsTer6
XR_001752427.1:n.3408del
XR_933973.2:n.3408del
NM_001163809.2:c.3256del MANE Select NP_001157281.1:p.Gln1086LysfsTer6
NM_001163811.2:c.-14-2165del NP_001157283.1:n.-14-2165del
NM_152348.4:c.103del NP_689561.2:p.Gln35LysfsTer6
NM_001163673.2:c.59-2165del NP_001157145.1:n.59-2165del