Canonical Allele Identifier: CA2635265479
Gene: WDR81 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1728509_1728512del , CM000679.2:g.1728509_1728512del GRCh38
NC_000017.10:g.1631803_1631806del , CM000679.1:g.1631803_1631806del GRCh37
NC_000017.9:g.1578553_1578556del NCBI36
NG_032811.1:g.16987_16990del

Transcript Alleles

HGVS Amino-acid Change
ENST00000409644.6:c.3550_3553del MANE Select ENSP00000386609.1:p.Ser1184ThrfsTer?
ENST00000309182.9:c.397_400del ENSP00000312074.5:p.Ser133ThrfsTer?
ENST00000409644.5:c.3550_3553del ENSP00000386609.1:p.Ser1184ThrfsTer?
ENST00000418841.5:c.-89+3723_-89+3726del ENSP00000395198.1:n.-89+3723_-89+3726del
ENST00000419248.5:c.-14-1871_-14-1868del ENSP00000407845.1:n.-14-1871_-14-1868del
ENST00000437219.6:c.59-1871_59-1868del ENSP00000391074.2:n.59-1871_59-1868del
ENST00000446363.5:c.-308-2246_-308-2243del ENSP00000401560.1:n.-308-2246_-308-2243del
ENST00000455636.5:c.59-1871_59-1868del ENSP00000395226.1:n.59-1871_59-1868del
ENST00000464528.5:n.936_939del
ENST00000468539.5:c.63-3816_63-3813del ENSP00000460742.1:n.63-3816_63-3813del
ENST00000492901.1:n.88-1871_88-1868del
ENST00000575206.1:c.300_303del
NM_001163673.1:c.59-1871_59-1868del NP_001157145.1:n.59-1871_59-1868del
NM_001163809.1:c.3550_3553del NP_001157281.1:p.Ser1184ThrfsTer?
NM_001163811.1:c.-14-1871_-14-1868del NP_001157283.1:n.-14-1871_-14-1868del
NM_152348.3:c.397_400del NP_689561.2:p.Ser133ThrfsTer?
XM_005256454.2:c.3550_3553del XP_005256511.1:p.Ser1184ThrfsTer?
XM_011523650.1:c.3550_3553del XP_011521952.1:p.Ser1184ThrfsTer?
XM_011523651.1:c.397_400del XP_011521953.1:p.Ser133ThrfsTer?
XR_933973.1:n.3694_3697del
XM_011523651.2:c.397_400del XP_011521953.1:p.Ser133ThrfsTer?
XM_017024184.1:c.3550_3553del XP_016879673.1:p.Ser1184ThrfsTer?
XR_001752427.1:n.3702_3705del
XR_933973.2:n.3702_3705del
NM_001163809.2:c.3550_3553del MANE Select NP_001157281.1:p.Ser1184ThrfsTer?
NM_001163811.2:c.-14-1871_-14-1868del NP_001157283.1:n.-14-1871_-14-1868del
NM_152348.4:c.397_400del NP_689561.2:p.Ser133ThrfsTer?
NM_001163673.2:c.59-1871_59-1868del NP_001157145.1:n.59-1871_59-1868del