Canonical Allele Identifier: CA1144056030
Gene: DCAF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168045162A= , CM000663.2:g.168045162A= GRCh38
NC_000001.10:g.168014400A= , CM000663.1:g.168014400A= GRCh37
NC_000001.9:g.166281024A= NCBI36
NG_053062.1:g.113924A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367840.4:c.2193A= MANE Select ENSP00000356814.3:p.Thr731=
ENST00000312263.10:c.1962A= ENSP00000311949.6:p.Thr654=
ENST00000367840.3:c.2193A= ENSP00000356814.3:p.Thr731=
ENST00000367843.7:c.2022A= ENSP00000356817.3:p.Thr674=
ENST00000432587.6:c.2100A= ENSP00000396238.2:p.Thr700=
ENST00000478668.1:n.82A=
ENST00000489398.1:n.761A=
NM_001017977.2:c.1962A= NP_001017977.1:p.Thr654=
NM_001198956.1:c.2193A= NP_001185885.1:p.Thr731=
NM_001198957.1:c.2100A= NP_001185886.1:p.Thr700=
NM_018442.3:c.2022A= NP_060912.2:p.Thr674=
XM_005245331.3:c.2193A= XP_005245388.1:p.Thr731=
XM_005245332.3:c.2022A= XP_005245389.1:p.Thr674=
XM_005245333.3:c.1962A= XP_005245390.1:p.Thr654=
XM_011509767.1:c.1752A= XP_011508069.1:p.Thr584=
XR_921892.1:n.2286A=
XR_921893.1:n.2115A=
NM_001349773.1:c.2193A= NP_001336702.1:p.Thr731=
NM_001349774.1:c.1581A= NP_001336703.1:p.Thr527=
NM_001349775.1:c.1581A= NP_001336704.1:p.Thr527=
NM_001349776.1:c.1581A= NP_001336705.1:p.Thr527=
NM_001349777.1:c.1581A= NP_001336706.1:p.Thr527=
NM_001349778.1:c.1521A= NP_001336707.1:p.Thr507=
NM_001349779.1:c.1521A= NP_001336708.1:p.Thr507=
NM_001349780.1:c.1521A= NP_001336709.1:p.Thr507=
NR_146228.1:n.1881A=
NR_146229.1:n.2498A=
NR_146230.1:n.2197A=
XM_005245332.5:c.2022A= XP_005245389.1:p.Thr674=
XM_005245333.5:c.1962A= XP_005245390.1:p.Thr654=
XM_017001779.2:c.1752A= XP_016857268.1:p.Thr584=
XM_024448371.1:c.1752A= XP_024304139.1:p.Thr584=
XM_024448372.1:c.1581A= XP_024304140.1:p.Thr527=
XM_024448373.1:c.1521A= XP_024304141.1:p.Thr507=
XM_024448374.1:c.1521A= XP_024304142.1:p.Thr507=
XM_024448375.1:c.1521A= XP_024304143.1:p.Thr507=
NM_001017977.3:c.1962A= NP_001017977.1:p.Thr654=
NM_001198956.2:c.2193A= MANE Select NP_001185885.1:p.Thr731=
NM_001198957.2:c.2100A= NP_001185886.1:p.Thr700=
NM_001349773.2:c.2193A= NP_001336702.1:p.Thr731=
NM_001349774.2:c.1581A= NP_001336703.1:p.Thr527=
NM_001349775.2:c.1581A= NP_001336704.1:p.Thr527=
NM_001349776.2:c.1581A= NP_001336705.1:p.Thr527=
NM_001349777.2:c.1581A= NP_001336706.1:p.Thr527=
NM_001349778.2:c.1521A= NP_001336707.1:p.Thr507=
NM_001349779.2:c.1521A= NP_001336708.1:p.Thr507=
NM_001349780.2:c.1521A= NP_001336709.1:p.Thr507=
NM_001393650.1:c.1962A= NP_001380579.1:p.Thr654=
NM_001393651.1:c.2022A= NP_001380580.1:p.Thr674=
NM_018442.4:c.2022A= NP_060912.2:p.Thr674=
NR_146228.2:n.1757A=
NR_146229.2:n.2374A=
NR_146230.2:n.2073A=