Canonical Allele Identifier: CA1205512905

Gene: DCAF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168045218C= , CM000663.2:g.168045218C=	GRCh38
NC_000001.10:g.168014456C= , CM000663.1:g.168014456C=	GRCh37
NC_000001.9:g.166281080C=	NCBI36
NG_053062.1:g.113980C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367840.4:c.2249C= MANE Select	ENSP00000356814.3:p.Pro750=
ENST00000312263.10:c.2018C=	ENSP00000311949.6:p.Pro673=
ENST00000367840.3:c.2249C=	ENSP00000356814.3:p.Pro750=
ENST00000367843.7:c.2078C=	ENSP00000356817.3:p.Pro693=
ENST00000432587.6:c.2156C=	ENSP00000396238.2:p.Pro719=
ENST00000478668.1:n.138C=
ENST00000489398.1:n.817C=
NM_001017977.2:c.2018C=	NP_001017977.1:p.Pro673=
NM_001198956.1:c.2249C=	NP_001185885.1:p.Pro750=
NM_001198957.1:c.2156C=	NP_001185886.1:p.Pro719=
NM_018442.3:c.2078C=	NP_060912.2:p.Pro693=
XM_005245331.3:c.2249C=	XP_005245388.1:p.Pro750=
XM_005245332.3:c.2078C=	XP_005245389.1:p.Pro693=
XM_005245333.3:c.2018C=	XP_005245390.1:p.Pro673=
XM_011509767.1:c.1808C=	XP_011508069.1:p.Pro603=
XR_921892.1:n.2342C=
XR_921893.1:n.2171C=
NM_001349773.1:c.2249C=	NP_001336702.1:p.Pro750=
NM_001349774.1:c.1637C=	NP_001336703.1:p.Pro546=
NM_001349775.1:c.1637C=	NP_001336704.1:p.Pro546=
NM_001349776.1:c.1637C=	NP_001336705.1:p.Pro546=
NM_001349777.1:c.1637C=	NP_001336706.1:p.Pro546=
NM_001349778.1:c.1577C=	NP_001336707.1:p.Pro526=
NM_001349779.1:c.1577C=	NP_001336708.1:p.Pro526=
NM_001349780.1:c.1577C=	NP_001336709.1:p.Pro526=
NR_146228.1:n.1937C=
NR_146229.1:n.2554C=
NR_146230.1:n.2253C=
XM_005245332.5:c.2078C=	XP_005245389.1:p.Pro693=
XM_005245333.5:c.2018C=	XP_005245390.1:p.Pro673=
XM_017001779.2:c.1808C=	XP_016857268.1:p.Pro603=
XM_024448371.1:c.1808C=	XP_024304139.1:p.Pro603=
XM_024448372.1:c.1637C=	XP_024304140.1:p.Pro546=
XM_024448373.1:c.1577C=	XP_024304141.1:p.Pro526=
XM_024448374.1:c.1577C=	XP_024304142.1:p.Pro526=
XM_024448375.1:c.1577C=	XP_024304143.1:p.Pro526=
NM_001017977.3:c.2018C=	NP_001017977.1:p.Pro673=
NM_001198956.2:c.2249C= MANE Select	NP_001185885.1:p.Pro750=
NM_001198957.2:c.2156C=	NP_001185886.1:p.Pro719=
NM_001349773.2:c.2249C=	NP_001336702.1:p.Pro750=
NM_001349774.2:c.1637C=	NP_001336703.1:p.Pro546=
NM_001349775.2:c.1637C=	NP_001336704.1:p.Pro546=
NM_001349776.2:c.1637C=	NP_001336705.1:p.Pro546=
NM_001349777.2:c.1637C=	NP_001336706.1:p.Pro546=
NM_001349778.2:c.1577C=	NP_001336707.1:p.Pro526=
NM_001349779.2:c.1577C=	NP_001336708.1:p.Pro526=
NM_001349780.2:c.1577C=	NP_001336709.1:p.Pro526=
NM_001393650.1:c.2018C=	NP_001380579.1:p.Pro673=
NM_001393651.1:c.2078C=	NP_001380580.1:p.Pro693=
NM_018442.4:c.2078C=	NP_060912.2:p.Pro693=
NR_146228.2:n.1813C=
NR_146229.2:n.2430C=
NR_146230.2:n.2129C=