Canonical Allele Identifier: CA1205512872
Gene: DCAF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168045112C= , CM000663.2:g.168045112C= GRCh38
NC_000001.10:g.168014350C= , CM000663.1:g.168014350C= GRCh37
NC_000001.9:g.166280974C= NCBI36
NG_053062.1:g.113874C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367840.4:c.2143C= MANE Select ENSP00000356814.3:p.Pro715=
ENST00000312263.10:c.1912C= ENSP00000311949.6:p.Pro638=
ENST00000367840.3:c.2143C= ENSP00000356814.3:p.Pro715=
ENST00000367843.7:c.1972C= ENSP00000356817.3:p.Pro658=
ENST00000432587.6:c.2050C= ENSP00000396238.2:p.Pro684=
ENST00000478668.1:n.32C=
ENST00000489398.1:n.711C=
NM_001017977.2:c.1912C= NP_001017977.1:p.Pro638=
NM_001198956.1:c.2143C= NP_001185885.1:p.Pro715=
NM_001198957.1:c.2050C= NP_001185886.1:p.Pro684=
NM_018442.3:c.1972C= NP_060912.2:p.Pro658=
XM_005245331.3:c.2143C= XP_005245388.1:p.Pro715=
XM_005245332.3:c.1972C= XP_005245389.1:p.Pro658=
XM_005245333.3:c.1912C= XP_005245390.1:p.Pro638=
XM_011509767.1:c.1702C= XP_011508069.1:p.Pro568=
XR_921892.1:n.2236C=
XR_921893.1:n.2065C=
NM_001349773.1:c.2143C= NP_001336702.1:p.Pro715=
NM_001349774.1:c.1531C= NP_001336703.1:p.Pro511=
NM_001349775.1:c.1531C= NP_001336704.1:p.Pro511=
NM_001349776.1:c.1531C= NP_001336705.1:p.Pro511=
NM_001349777.1:c.1531C= NP_001336706.1:p.Pro511=
NM_001349778.1:c.1471C= NP_001336707.1:p.Pro491=
NM_001349779.1:c.1471C= NP_001336708.1:p.Pro491=
NM_001349780.1:c.1471C= NP_001336709.1:p.Pro491=
NR_146228.1:n.1831C=
NR_146229.1:n.2448C=
NR_146230.1:n.2147C=
XM_005245332.5:c.1972C= XP_005245389.1:p.Pro658=
XM_005245333.5:c.1912C= XP_005245390.1:p.Pro638=
XM_017001779.2:c.1702C= XP_016857268.1:p.Pro568=
XM_024448371.1:c.1702C= XP_024304139.1:p.Pro568=
XM_024448372.1:c.1531C= XP_024304140.1:p.Pro511=
XM_024448373.1:c.1471C= XP_024304141.1:p.Pro491=
XM_024448374.1:c.1471C= XP_024304142.1:p.Pro491=
XM_024448375.1:c.1471C= XP_024304143.1:p.Pro491=
NM_001017977.3:c.1912C= NP_001017977.1:p.Pro638=
NM_001198956.2:c.2143C= MANE Select NP_001185885.1:p.Pro715=
NM_001198957.2:c.2050C= NP_001185886.1:p.Pro684=
NM_001349773.2:c.2143C= NP_001336702.1:p.Pro715=
NM_001349774.2:c.1531C= NP_001336703.1:p.Pro511=
NM_001349775.2:c.1531C= NP_001336704.1:p.Pro511=
NM_001349776.2:c.1531C= NP_001336705.1:p.Pro511=
NM_001349777.2:c.1531C= NP_001336706.1:p.Pro511=
NM_001349778.2:c.1471C= NP_001336707.1:p.Pro491=
NM_001349779.2:c.1471C= NP_001336708.1:p.Pro491=
NM_001349780.2:c.1471C= NP_001336709.1:p.Pro491=
NM_001393650.1:c.1912C= NP_001380579.1:p.Pro638=
NM_001393651.1:c.1972C= NP_001380580.1:p.Pro658=
NM_018442.4:c.1972C= NP_060912.2:p.Pro658=
NR_146228.2:n.1707C=
NR_146229.2:n.2324C=
NR_146230.2:n.2023C=