Canonical Allele Identifier: CA8273198
Gene: WDR81 HGNC NCBI

Linked Data

ClinVar Variation Id: 2230336
ClinVar RCV Id: RCV002702777
dbSNP Id: rs747069460
gnomAD v2: 17-1631441-G-T
gnomAD v3: 17-1728147-G-T
gnomAD v4: 17-1728147-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1728147G>T , CM000679.2:g.1728147G>T GRCh38
NC_000017.10:g.1631441G>T , CM000679.1:g.1631441G>T GRCh37
NC_000017.9:g.1578191G>T NCBI36
NG_032811.1:g.16625G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409644.6:c.3188G>T MANE Select ENSP00000386609.1:p.Gly1063Val
ENST00000309182.9:c.35G>T ENSP00000312074.5:p.Gly12Val
ENST00000409644.5:c.3188G>T ENSP00000386609.1:p.Gly1063Val
ENST00000418841.5:c.-89+3361G>T ENSP00000395198.1:n.-89+3361G>T
ENST00000419248.5:c.-14-2233G>T ENSP00000407845.1:n.-14-2233G>T
ENST00000437219.6:c.59-2233G>T ENSP00000391074.2:n.59-2233G>T
ENST00000446363.5:c.-308-2608G>T ENSP00000401560.1:n.-308-2608G>T
ENST00000455636.5:c.59-2233G>T ENSP00000395226.1:n.59-2233G>T
ENST00000464528.5:n.574G>T
ENST00000468539.5:c.63-4178G>T ENSP00000460742.1:n.63-4178G>T
ENST00000492901.1:n.88-2233G>T
NM_001163673.1:c.59-2233G>T NP_001157145.1:n.59-2233G>T
NM_001163809.1:c.3188G>T NP_001157281.1:p.Gly1063Val
NM_001163811.1:c.-14-2233G>T NP_001157283.1:n.-14-2233G>T
NM_152348.3:c.35G>T NP_689561.2:p.Gly12Val
XM_005256454.2:c.3188G>T XP_005256511.1:p.Gly1063Val
XM_011523650.1:c.3188G>T XP_011521952.1:p.Gly1063Val
XM_011523651.1:c.35G>T XP_011521953.1:p.Gly12Val
XR_933973.1:n.3332G>T
XM_011523651.2:c.35G>T XP_011521953.1:p.Gly12Val
XM_017024184.1:c.3188G>T XP_016879673.1:p.Gly1063Val
XR_001752427.1:n.3340G>T
XR_933973.2:n.3340G>T
NM_001163809.2:c.3188G>T MANE Select NP_001157281.1:p.Gly1063Val
NM_001163811.2:c.-14-2233G>T NP_001157283.1:n.-14-2233G>T
NM_152348.4:c.35G>T NP_689561.2:p.Gly12Val
NM_001163673.2:c.59-2233G>T NP_001157145.1:n.59-2233G>T