Canonical Allele Identifier: CA343085169

Gene: DCAF6

Linked Data

• MyVariant Identifiers: chr1:g.168014396A>T (hg19) ; chr1:g.168045158A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168045158A>T , CM000663.2:g.168045158A>T	GRCh38
NC_000001.10:g.168014396A>T , CM000663.1:g.168014396A>T	GRCh37
NC_000001.9:g.166281020A>T	NCBI36
NG_053062.1:g.113920A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367840.4:c.2189A>T MANE Select	ENSP00000356814.3:p.Asp730Val
ENST00000312263.10:c.1958A>T	ENSP00000311949.6:p.Asp653Val
ENST00000367840.3:c.2189A>T	ENSP00000356814.3:p.Asp730Val
ENST00000367843.7:c.2018A>T	ENSP00000356817.3:p.Asp673Val
ENST00000432587.6:c.2096A>T	ENSP00000396238.2:p.Asp699Val
ENST00000478668.1:n.78A>T
ENST00000489398.1:n.757A>T
NM_001017977.2:c.1958A>T	NP_001017977.1:p.Asp653Val
NM_001198956.1:c.2189A>T	NP_001185885.1:p.Asp730Val
NM_001198957.1:c.2096A>T	NP_001185886.1:p.Asp699Val
NM_018442.3:c.2018A>T	NP_060912.2:p.Asp673Val
XM_005245331.3:c.2189A>T	XP_005245388.1:p.Asp730Val
XM_005245332.3:c.2018A>T	XP_005245389.1:p.Asp673Val
XM_005245333.3:c.1958A>T	XP_005245390.1:p.Asp653Val
XM_011509767.1:c.1748A>T	XP_011508069.1:p.Asp583Val
XR_921892.1:n.2282A>T
XR_921893.1:n.2111A>T
NM_001349773.1:c.2189A>T	NP_001336702.1:p.Asp730Val
NM_001349774.1:c.1577A>T	NP_001336703.1:p.Asp526Val
NM_001349775.1:c.1577A>T	NP_001336704.1:p.Asp526Val
NM_001349776.1:c.1577A>T	NP_001336705.1:p.Asp526Val
NM_001349777.1:c.1577A>T	NP_001336706.1:p.Asp526Val
NM_001349778.1:c.1517A>T	NP_001336707.1:p.Asp506Val
NM_001349779.1:c.1517A>T	NP_001336708.1:p.Asp506Val
NM_001349780.1:c.1517A>T	NP_001336709.1:p.Asp506Val
NR_146228.1:n.1877A>T
NR_146229.1:n.2494A>T
NR_146230.1:n.2193A>T
XM_005245332.5:c.2018A>T	XP_005245389.1:p.Asp673Val
XM_005245333.5:c.1958A>T	XP_005245390.1:p.Asp653Val
XM_017001779.2:c.1748A>T	XP_016857268.1:p.Asp583Val
XM_024448371.1:c.1748A>T	XP_024304139.1:p.Asp583Val
XM_024448372.1:c.1577A>T	XP_024304140.1:p.Asp526Val
XM_024448373.1:c.1517A>T	XP_024304141.1:p.Asp506Val
XM_024448374.1:c.1517A>T	XP_024304142.1:p.Asp506Val
XM_024448375.1:c.1517A>T	XP_024304143.1:p.Asp506Val
NM_001017977.3:c.1958A>T	NP_001017977.1:p.Asp653Val
NM_001198956.2:c.2189A>T MANE Select	NP_001185885.1:p.Asp730Val
NM_001198957.2:c.2096A>T	NP_001185886.1:p.Asp699Val
NM_001349773.2:c.2189A>T	NP_001336702.1:p.Asp730Val
NM_001349774.2:c.1577A>T	NP_001336703.1:p.Asp526Val
NM_001349775.2:c.1577A>T	NP_001336704.1:p.Asp526Val
NM_001349776.2:c.1577A>T	NP_001336705.1:p.Asp526Val
NM_001349777.2:c.1577A>T	NP_001336706.1:p.Asp526Val
NM_001349778.2:c.1517A>T	NP_001336707.1:p.Asp506Val
NM_001349779.2:c.1517A>T	NP_001336708.1:p.Asp506Val
NM_001349780.2:c.1517A>T	NP_001336709.1:p.Asp506Val
NM_001393650.1:c.1958A>T	NP_001380579.1:p.Asp653Val
NM_001393651.1:c.2018A>T	NP_001380580.1:p.Asp673Val
NM_018442.4:c.2018A>T	NP_060912.2:p.Asp673Val
NR_146228.2:n.1753A>T
NR_146229.2:n.2370A>T
NR_146230.2:n.2069A>T