Canonical Allele Identifier: CA8273216

Gene: WDR81

Linked Data

• ClinVar Variation Id: 2317295
• ClinVar RCV Id: RCV002897982
• dbSNP Id: rs780141508
• ExAC: 17:1631515 G / C
• gnomAD v2: 17-1631515-G-C
• gnomAD v3: 17-1728221-G-C
• gnomAD v4: 17-1728221-G-C
• MyVariant Identifiers: chr17:g.1631515G>C (hg19) ; chr17:g.1728221G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1728221G>C , CM000679.2:g.1728221G>C	GRCh38
NC_000017.10:g.1631515G>C , CM000679.1:g.1631515G>C	GRCh37
NC_000017.9:g.1578265G>C	NCBI36
NG_032811.1:g.16699G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409644.6:c.3262G>C MANE Select	ENSP00000386609.1:p.Gly1088Arg
ENST00000309182.9:c.109G>C	ENSP00000312074.5:p.Gly37Arg
ENST00000409644.5:c.3262G>C	ENSP00000386609.1:p.Gly1088Arg
ENST00000418841.5:c.-89+3435G>C	ENSP00000395198.1:n.-89+3435G>C
ENST00000419248.5:c.-14-2159G>C	ENSP00000407845.1:n.-14-2159G>C
ENST00000437219.6:c.59-2159G>C	ENSP00000391074.2:n.59-2159G>C
ENST00000446363.5:c.-308-2534G>C	ENSP00000401560.1:n.-308-2534G>C
ENST00000455636.5:c.59-2159G>C	ENSP00000395226.1:n.59-2159G>C
ENST00000464528.5:n.648G>C
ENST00000468539.5:c.63-4104G>C	ENSP00000460742.1:n.63-4104G>C
ENST00000492901.1:n.88-2159G>C
ENST00000575206.1:c.12G>C
NM_001163673.1:c.59-2159G>C	NP_001157145.1:n.59-2159G>C
NM_001163809.1:c.3262G>C	NP_001157281.1:p.Gly1088Arg
NM_001163811.1:c.-14-2159G>C	NP_001157283.1:n.-14-2159G>C
NM_152348.3:c.109G>C	NP_689561.2:p.Gly37Arg
XM_005256454.2:c.3262G>C	XP_005256511.1:p.Gly1088Arg
XM_011523650.1:c.3262G>C	XP_011521952.1:p.Gly1088Arg
XM_011523651.1:c.109G>C	XP_011521953.1:p.Gly37Arg
XR_933973.1:n.3406G>C
XM_011523651.2:c.109G>C	XP_011521953.1:p.Gly37Arg
XM_017024184.1:c.3262G>C	XP_016879673.1:p.Gly1088Arg
XR_001752427.1:n.3414G>C
XR_933973.2:n.3414G>C
NM_001163809.2:c.3262G>C MANE Select	NP_001157281.1:p.Gly1088Arg
NM_001163811.2:c.-14-2159G>C	NP_001157283.1:n.-14-2159G>C
NM_152348.4:c.109G>C	NP_689561.2:p.Gly37Arg
NM_001163673.2:c.59-2159G>C	NP_001157145.1:n.59-2159G>C