Canonical Allele Identifier: CA357934
Gene: DCAF6 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 224814
ClinVar RCV Id: RCV000210411
dbSNP Id: rs145189179

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168045209G>A , CM000663.2:g.168045209G>A GRCh38
NC_000001.10:g.168014447G>A , CM000663.1:g.168014447G>A GRCh37
NC_000001.9:g.166281071G>A NCBI36
NG_053062.1:g.113971G>A

Transcript Alleles

HGVS Amino-acid change
NM_001017977.2:c.2009G>A VV NP_001017977.1:p.Arg670Gln
NM_001198956.1:c.2240G>A VV NP_001185885.1:p.Arg747Gln
NM_001198957.1:c.2147G>A VV NP_001185886.1:p.Arg716Gln
NM_018442.3:c.2069G>A VV NP_060912.2:p.Arg690Gln
XM_005245331.3:c.2240G>A XP_005245388.1:p.Arg747Gln
XM_005245332.3:c.2069G>A XP_005245389.1:p.Arg690Gln
XM_005245333.3:c.2009G>A XP_005245390.1:p.Arg670Gln
XM_011509767.1:c.1799G>A XP_011508069.1:p.Arg600Gln
XR_921892.1:n.2333G>A
XR_921893.1:n.2162G>A
NM_001349773.1:c.2240G>A VV NP_001336702.1:p.Arg747Gln
NM_001349774.1:c.1628G>A VV NP_001336703.1:p.Arg543Gln
NM_001349775.1:c.1628G>A VV NP_001336704.1:p.Arg543Gln
NM_001349776.1:c.1628G>A VV NP_001336705.1:p.Arg543Gln
NM_001349777.1:c.1628G>A VV NP_001336706.1:p.Arg543Gln
NM_001349778.1:c.1568G>A VV NP_001336707.1:p.Arg523Gln
NM_001349779.1:c.1568G>A VV NP_001336708.1:p.Arg523Gln
NM_001349780.1:c.1568G>A VV NP_001336709.1:p.Arg523Gln
NR_146228.1:n.1928G>A
NR_146229.1:n.2545G>A
NR_146230.1:n.2244G>A
XM_005245332.5:c.2069G>A
XM_005245333.5:c.2009G>A
XM_017001779.2:c.1799G>A XP_016857268.1:p.Arg600Gln
XM_024448371.1:c.1799G>A XP_024304139.1:p.Arg600Gln
XM_024448372.1:c.1628G>A XP_024304140.1:p.Arg543Gln
XM_024448373.1:c.1568G>A XP_024304141.1:p.Arg523Gln
XM_024448374.1:c.1568G>A XP_024304142.1:p.Arg523Gln
XM_024448375.1:c.1568G>A XP_024304143.1:p.Arg523Gln
ENST00000312263.10:c.2009G>A ENSP00000311949.6:p.Arg670Gln
ENST00000367840.3:c.2240G>A ENSP00000356814.3:p.Arg747Gln
ENST00000367843.7:c.2069G>A ENSP00000356817.3:p.Arg690Gln
ENST00000432587.6:c.2147G>A ENSP00000396238.2:p.Arg716Gln
ENST00000478668.1:n.129G>A
ENST00000489398.1:n.808G>A