Canonical Allele Identifier: CA421704953

Gene: DCAF6

Linked Data

• MyVariant Identifiers: chr1:g.168014358T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168045120T>A , CM000663.2:g.168045120T>A	GRCh38
NC_000001.10:g.168014358T>A , CM000663.1:g.168014358T>A	GRCh37
NC_000001.9:g.166280982T>A	NCBI36
NG_053062.1:g.113882T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367840.4:c.2151T>A MANE Select	ENSP00000356814.3:p.Ala717=
ENST00000312263.10:c.1920T>A	ENSP00000311949.6:p.Ala640=
ENST00000367840.3:c.2151T>A	ENSP00000356814.3:p.Ala717=
ENST00000367843.7:c.1980T>A	ENSP00000356817.3:p.Ala660=
ENST00000432587.6:c.2058T>A	ENSP00000396238.2:p.Ala686=
ENST00000478668.1:n.40T>A
ENST00000489398.1:n.719T>A
NM_001017977.2:c.1920T>A	NP_001017977.1:p.Ala640=
NM_001198956.1:c.2151T>A	NP_001185885.1:p.Ala717=
NM_001198957.1:c.2058T>A	NP_001185886.1:p.Ala686=
NM_018442.3:c.1980T>A	NP_060912.2:p.Ala660=
XM_005245331.3:c.2151T>A	XP_005245388.1:p.Ala717=
XM_005245332.3:c.1980T>A	XP_005245389.1:p.Ala660=
XM_005245333.3:c.1920T>A	XP_005245390.1:p.Ala640=
XM_011509767.1:c.1710T>A	XP_011508069.1:p.Ala570=
XR_921892.1:n.2244T>A
XR_921893.1:n.2073T>A
NM_001349773.1:c.2151T>A	NP_001336702.1:p.Ala717=
NM_001349774.1:c.1539T>A	NP_001336703.1:p.Ala513=
NM_001349775.1:c.1539T>A	NP_001336704.1:p.Ala513=
NM_001349776.1:c.1539T>A	NP_001336705.1:p.Ala513=
NM_001349777.1:c.1539T>A	NP_001336706.1:p.Ala513=
NM_001349778.1:c.1479T>A	NP_001336707.1:p.Ala493=
NM_001349779.1:c.1479T>A	NP_001336708.1:p.Ala493=
NM_001349780.1:c.1479T>A	NP_001336709.1:p.Ala493=
NR_146228.1:n.1839T>A
NR_146229.1:n.2456T>A
NR_146230.1:n.2155T>A
XM_005245332.5:c.1980T>A	XP_005245389.1:p.Ala660=
XM_005245333.5:c.1920T>A	XP_005245390.1:p.Ala640=
XM_017001779.2:c.1710T>A	XP_016857268.1:p.Ala570=
XM_024448371.1:c.1710T>A	XP_024304139.1:p.Ala570=
XM_024448372.1:c.1539T>A	XP_024304140.1:p.Ala513=
XM_024448373.1:c.1479T>A	XP_024304141.1:p.Ala493=
XM_024448374.1:c.1479T>A	XP_024304142.1:p.Ala493=
XM_024448375.1:c.1479T>A	XP_024304143.1:p.Ala493=
NM_001017977.3:c.1920T>A	NP_001017977.1:p.Ala640=
NM_001198956.2:c.2151T>A MANE Select	NP_001185885.1:p.Ala717=
NM_001198957.2:c.2058T>A	NP_001185886.1:p.Ala686=
NM_001349773.2:c.2151T>A	NP_001336702.1:p.Ala717=
NM_001349774.2:c.1539T>A	NP_001336703.1:p.Ala513=
NM_001349775.2:c.1539T>A	NP_001336704.1:p.Ala513=
NM_001349776.2:c.1539T>A	NP_001336705.1:p.Ala513=
NM_001349777.2:c.1539T>A	NP_001336706.1:p.Ala513=
NM_001349778.2:c.1479T>A	NP_001336707.1:p.Ala493=
NM_001349779.2:c.1479T>A	NP_001336708.1:p.Ala493=
NM_001349780.2:c.1479T>A	NP_001336709.1:p.Ala493=
NM_001393650.1:c.1920T>A	NP_001380579.1:p.Ala640=
NM_001393651.1:c.1980T>A	NP_001380580.1:p.Ala660=
NM_018442.4:c.1980T>A	NP_060912.2:p.Ala660=
NR_146228.2:n.1715T>A
NR_146229.2:n.2332T>A
NR_146230.2:n.2031T>A