Canonical Allele Identifier: CA16607602
Gene: WDR81 HGNC NCBI

Linked Data

ClinVar Variation Id: 392796
ClinVar RCV Id: RCV000426986
dbSNP Id: rs1057524638
MyVariant Identifiers: chr17:g.1629817C>T (hg19) chr17:g.1726523C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1726523C>T , CM000679.2:g.1726523C>T GRCh38
NC_000017.10:g.1629817C>T , CM000679.1:g.1629817C>T GRCh37
NC_000017.9:g.1576567C>T NCBI36
NG_032811.1:g.15001C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000409644.6:c.1564C>T MANE Select ENSP00000386609.1:p.Gln522Ter
ENST00000309182.9:c.-123-1467C>T ENSP00000312074.5:n.-123-1467C>T
ENST00000409644.5:c.1564C>T ENSP00000386609.1:p.Gln522Ter
ENST00000418841.5:c.-89+1737C>T ENSP00000395198.1:n.-89+1737C>T
ENST00000419248.5:c.-15+1737C>T ENSP00000407845.1:n.-15+1737C>T
ENST00000437219.6:c.59-3857C>T ENSP00000391074.2:n.59-3857C>T
ENST00000446363.5:c.-308-4232C>T ENSP00000401560.1:n.-308-4232C>T
ENST00000455636.5:c.59-3857C>T ENSP00000395226.1:n.59-3857C>T
ENST00000468539.5:c.63-5802C>T ENSP00000460742.1:n.63-5802C>T
ENST00000492901.1:n.88-3857C>T
NM_001163673.1:c.59-3857C>T NP_001157145.1:n.59-3857C>T
NM_001163809.1:c.1564C>T NP_001157281.1:p.Gln522Ter
NM_001163811.1:c.-15+1737C>T NP_001157283.1:n.-15+1737C>T
NM_152348.3:c.-123-1467C>T NP_689561.2:n.-123-1467C>T
XM_005256454.2:c.1564C>T XP_005256511.1:p.Gln522Ter
XM_011523650.1:c.1564C>T XP_011521952.1:p.Gln522Ter
XM_011523651.1:c.-123-1467C>T XP_011521953.1:n.-123-1467C>T
XR_933973.1:n.1708C>T
XM_011523651.2:c.-123-1467C>T XP_011521953.1:n.-123-1467C>T
XM_017024184.1:c.1564C>T XP_016879673.1:p.Gln522Ter
XR_001752427.1:n.1716C>T
XR_933973.2:n.1716C>T
NM_001163809.2:c.1564C>T MANE Select NP_001157281.1:p.Gln522Ter
NM_001163811.2:c.-15+1737C>T NP_001157283.1:n.-15+1737C>T
NM_152348.4:c.-123-1467C>T NP_689561.2:n.-123-1467C>T
NM_001163673.2:c.59-3857C>T NP_001157145.1:n.59-3857C>T
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