Canonical Allele Identifier: CA421705100

Gene: DCAF6

Linked Data

• MyVariant Identifiers: chr1:g.168014440A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168045202A>C , CM000663.2:g.168045202A>C	GRCh38
NC_000001.10:g.168014440A>C , CM000663.1:g.168014440A>C	GRCh37
NC_000001.9:g.166281064A>C	NCBI36
NG_053062.1:g.113964A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367840.4:c.2233A>C MANE Select	ENSP00000356814.3:p.Arg745=
ENST00000312263.10:c.2002A>C	ENSP00000311949.6:p.Arg668=
ENST00000367840.3:c.2233A>C	ENSP00000356814.3:p.Arg745=
ENST00000367843.7:c.2062A>C	ENSP00000356817.3:p.Arg688=
ENST00000432587.6:c.2140A>C	ENSP00000396238.2:p.Arg714=
ENST00000478668.1:n.122A>C
ENST00000489398.1:n.801A>C
NM_001017977.2:c.2002A>C	NP_001017977.1:p.Arg668=
NM_001198956.1:c.2233A>C	NP_001185885.1:p.Arg745=
NM_001198957.1:c.2140A>C	NP_001185886.1:p.Arg714=
NM_018442.3:c.2062A>C	NP_060912.2:p.Arg688=
XM_005245331.3:c.2233A>C	XP_005245388.1:p.Arg745=
XM_005245332.3:c.2062A>C	XP_005245389.1:p.Arg688=
XM_005245333.3:c.2002A>C	XP_005245390.1:p.Arg668=
XM_011509767.1:c.1792A>C	XP_011508069.1:p.Arg598=
XR_921892.1:n.2326A>C
XR_921893.1:n.2155A>C
NM_001349773.1:c.2233A>C	NP_001336702.1:p.Arg745=
NM_001349774.1:c.1621A>C	NP_001336703.1:p.Arg541=
NM_001349775.1:c.1621A>C	NP_001336704.1:p.Arg541=
NM_001349776.1:c.1621A>C	NP_001336705.1:p.Arg541=
NM_001349777.1:c.1621A>C	NP_001336706.1:p.Arg541=
NM_001349778.1:c.1561A>C	NP_001336707.1:p.Arg521=
NM_001349779.1:c.1561A>C	NP_001336708.1:p.Arg521=
NM_001349780.1:c.1561A>C	NP_001336709.1:p.Arg521=
NR_146228.1:n.1921A>C
NR_146229.1:n.2538A>C
NR_146230.1:n.2237A>C
XM_005245332.5:c.2062A>C	XP_005245389.1:p.Arg688=
XM_005245333.5:c.2002A>C	XP_005245390.1:p.Arg668=
XM_017001779.2:c.1792A>C	XP_016857268.1:p.Arg598=
XM_024448371.1:c.1792A>C	XP_024304139.1:p.Arg598=
XM_024448372.1:c.1621A>C	XP_024304140.1:p.Arg541=
XM_024448373.1:c.1561A>C	XP_024304141.1:p.Arg521=
XM_024448374.1:c.1561A>C	XP_024304142.1:p.Arg521=
XM_024448375.1:c.1561A>C	XP_024304143.1:p.Arg521=
NM_001017977.3:c.2002A>C	NP_001017977.1:p.Arg668=
NM_001198956.2:c.2233A>C MANE Select	NP_001185885.1:p.Arg745=
NM_001198957.2:c.2140A>C	NP_001185886.1:p.Arg714=
NM_001349773.2:c.2233A>C	NP_001336702.1:p.Arg745=
NM_001349774.2:c.1621A>C	NP_001336703.1:p.Arg541=
NM_001349775.2:c.1621A>C	NP_001336704.1:p.Arg541=
NM_001349776.2:c.1621A>C	NP_001336705.1:p.Arg541=
NM_001349777.2:c.1621A>C	NP_001336706.1:p.Arg541=
NM_001349778.2:c.1561A>C	NP_001336707.1:p.Arg521=
NM_001349779.2:c.1561A>C	NP_001336708.1:p.Arg521=
NM_001349780.2:c.1561A>C	NP_001336709.1:p.Arg521=
NM_001393650.1:c.2002A>C	NP_001380579.1:p.Arg668=
NM_001393651.1:c.2062A>C	NP_001380580.1:p.Arg688=
NM_018442.4:c.2062A>C	NP_060912.2:p.Arg688=
NR_146228.2:n.1797A>C
NR_146229.2:n.2414A>C
NR_146230.2:n.2113A>C