Canonical Allele Identifier: CA343084970

Gene: DCAF6

Linked Data

• MyVariant Identifiers: chr1:g.168014356G>A (hg19) ; chr1:g.168045118G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168045118G>A , CM000663.2:g.168045118G>A	GRCh38
NC_000001.10:g.168014356G>A , CM000663.1:g.168014356G>A	GRCh37
NC_000001.9:g.166280980G>A	NCBI36
NG_053062.1:g.113880G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367840.4:c.2149G>A MANE Select	ENSP00000356814.3:p.Ala717Thr
ENST00000312263.10:c.1918G>A	ENSP00000311949.6:p.Ala640Thr
ENST00000367840.3:c.2149G>A	ENSP00000356814.3:p.Ala717Thr
ENST00000367843.7:c.1978G>A	ENSP00000356817.3:p.Ala660Thr
ENST00000432587.6:c.2056G>A	ENSP00000396238.2:p.Ala686Thr
ENST00000478668.1:n.38G>A
ENST00000489398.1:n.717G>A
NM_001017977.2:c.1918G>A	NP_001017977.1:p.Ala640Thr
NM_001198956.1:c.2149G>A	NP_001185885.1:p.Ala717Thr
NM_001198957.1:c.2056G>A	NP_001185886.1:p.Ala686Thr
NM_018442.3:c.1978G>A	NP_060912.2:p.Ala660Thr
XM_005245331.3:c.2149G>A	XP_005245388.1:p.Ala717Thr
XM_005245332.3:c.1978G>A	XP_005245389.1:p.Ala660Thr
XM_005245333.3:c.1918G>A	XP_005245390.1:p.Ala640Thr
XM_011509767.1:c.1708G>A	XP_011508069.1:p.Ala570Thr
XR_921892.1:n.2242G>A
XR_921893.1:n.2071G>A
NM_001349773.1:c.2149G>A	NP_001336702.1:p.Ala717Thr
NM_001349774.1:c.1537G>A	NP_001336703.1:p.Ala513Thr
NM_001349775.1:c.1537G>A	NP_001336704.1:p.Ala513Thr
NM_001349776.1:c.1537G>A	NP_001336705.1:p.Ala513Thr
NM_001349777.1:c.1537G>A	NP_001336706.1:p.Ala513Thr
NM_001349778.1:c.1477G>A	NP_001336707.1:p.Ala493Thr
NM_001349779.1:c.1477G>A	NP_001336708.1:p.Ala493Thr
NM_001349780.1:c.1477G>A	NP_001336709.1:p.Ala493Thr
NR_146228.1:n.1837G>A
NR_146229.1:n.2454G>A
NR_146230.1:n.2153G>A
XM_005245332.5:c.1978G>A	XP_005245389.1:p.Ala660Thr
XM_005245333.5:c.1918G>A	XP_005245390.1:p.Ala640Thr
XM_017001779.2:c.1708G>A	XP_016857268.1:p.Ala570Thr
XM_024448371.1:c.1708G>A	XP_024304139.1:p.Ala570Thr
XM_024448372.1:c.1537G>A	XP_024304140.1:p.Ala513Thr
XM_024448373.1:c.1477G>A	XP_024304141.1:p.Ala493Thr
XM_024448374.1:c.1477G>A	XP_024304142.1:p.Ala493Thr
XM_024448375.1:c.1477G>A	XP_024304143.1:p.Ala493Thr
NM_001017977.3:c.1918G>A	NP_001017977.1:p.Ala640Thr
NM_001198956.2:c.2149G>A MANE Select	NP_001185885.1:p.Ala717Thr
NM_001198957.2:c.2056G>A	NP_001185886.1:p.Ala686Thr
NM_001349773.2:c.2149G>A	NP_001336702.1:p.Ala717Thr
NM_001349774.2:c.1537G>A	NP_001336703.1:p.Ala513Thr
NM_001349775.2:c.1537G>A	NP_001336704.1:p.Ala513Thr
NM_001349776.2:c.1537G>A	NP_001336705.1:p.Ala513Thr
NM_001349777.2:c.1537G>A	NP_001336706.1:p.Ala513Thr
NM_001349778.2:c.1477G>A	NP_001336707.1:p.Ala493Thr
NM_001349779.2:c.1477G>A	NP_001336708.1:p.Ala493Thr
NM_001349780.2:c.1477G>A	NP_001336709.1:p.Ala493Thr
NM_001393650.1:c.1918G>A	NP_001380579.1:p.Ala640Thr
NM_001393651.1:c.1978G>A	NP_001380580.1:p.Ala660Thr
NM_018442.4:c.1978G>A	NP_060912.2:p.Ala660Thr
NR_146228.2:n.1713G>A
NR_146229.2:n.2330G>A
NR_146230.2:n.2029G>A