Canonical Allele Identifier: CA343085431

Gene: DCAF6

Linked Data

• MyVariant Identifiers: chr1:g.168014440A>T (hg19) ; chr1:g.168045202A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367840.4:c.2233A>T MANE Select	ENSP00000356814.3:p.Arg745Trp
ENST00000312263.10:c.2002A>T	ENSP00000311949.6:p.Arg668Trp
ENST00000367840.3:c.2233A>T	ENSP00000356814.3:p.Arg745Trp
ENST00000367843.7:c.2062A>T	ENSP00000356817.3:p.Arg688Trp
ENST00000432587.6:c.2140A>T	ENSP00000396238.2:p.Arg714Trp
ENST00000478668.1:n.122A>T
ENST00000489398.1:n.801A>T
NM_001017977.2:c.2002A>T	NP_001017977.1:p.Arg668Trp
NM_001198956.1:c.2233A>T	NP_001185885.1:p.Arg745Trp
NM_001198957.1:c.2140A>T	NP_001185886.1:p.Arg714Trp
NM_018442.3:c.2062A>T	NP_060912.2:p.Arg688Trp
XM_005245331.3:c.2233A>T	XP_005245388.1:p.Arg745Trp
XM_005245332.3:c.2062A>T	XP_005245389.1:p.Arg688Trp
XM_005245333.3:c.2002A>T	XP_005245390.1:p.Arg668Trp
XM_011509767.1:c.1792A>T	XP_011508069.1:p.Arg598Trp
XR_921892.1:n.2326A>T
XR_921893.1:n.2155A>T
NM_001349773.1:c.2233A>T	NP_001336702.1:p.Arg745Trp
NM_001349774.1:c.1621A>T	NP_001336703.1:p.Arg541Trp
NM_001349775.1:c.1621A>T	NP_001336704.1:p.Arg541Trp
NM_001349776.1:c.1621A>T	NP_001336705.1:p.Arg541Trp
NM_001349777.1:c.1621A>T	NP_001336706.1:p.Arg541Trp
NM_001349778.1:c.1561A>T	NP_001336707.1:p.Arg521Trp
NM_001349779.1:c.1561A>T	NP_001336708.1:p.Arg521Trp
NM_001349780.1:c.1561A>T	NP_001336709.1:p.Arg521Trp
NR_146228.1:n.1921A>T
NR_146229.1:n.2538A>T
NR_146230.1:n.2237A>T
XM_005245332.5:c.2062A>T	XP_005245389.1:p.Arg688Trp
XM_005245333.5:c.2002A>T	XP_005245390.1:p.Arg668Trp
XM_017001779.2:c.1792A>T	XP_016857268.1:p.Arg598Trp
XM_024448371.1:c.1792A>T	XP_024304139.1:p.Arg598Trp
XM_024448372.1:c.1621A>T	XP_024304140.1:p.Arg541Trp
XM_024448373.1:c.1561A>T	XP_024304141.1:p.Arg521Trp
XM_024448374.1:c.1561A>T	XP_024304142.1:p.Arg521Trp
XM_024448375.1:c.1561A>T	XP_024304143.1:p.Arg521Trp
NM_001017977.3:c.2002A>T	NP_001017977.1:p.Arg668Trp
NM_001198956.2:c.2233A>T MANE Select	NP_001185885.1:p.Arg745Trp
NM_001198957.2:c.2140A>T	NP_001185886.1:p.Arg714Trp
NM_001349773.2:c.2233A>T	NP_001336702.1:p.Arg745Trp
NM_001349774.2:c.1621A>T	NP_001336703.1:p.Arg541Trp
NM_001349775.2:c.1621A>T	NP_001336704.1:p.Arg541Trp
NM_001349776.2:c.1621A>T	NP_001336705.1:p.Arg541Trp
NM_001349777.2:c.1621A>T	NP_001336706.1:p.Arg541Trp
NM_001349778.2:c.1561A>T	NP_001336707.1:p.Arg521Trp
NM_001349779.2:c.1561A>T	NP_001336708.1:p.Arg521Trp
NM_001349780.2:c.1561A>T	NP_001336709.1:p.Arg521Trp
NM_001393650.1:c.2002A>T	NP_001380579.1:p.Arg668Trp
NM_001393651.1:c.2062A>T	NP_001380580.1:p.Arg688Trp
NM_018442.4:c.2062A>T	NP_060912.2:p.Arg688Trp
NR_146228.2:n.1797A>T
NR_146229.2:n.2414A>T
NR_146230.2:n.2113A>T