Canonical Allele Identifier: CA343085048

Gene: DCAF6

Linked Data

• gnomAD v4: 1-168045137-C-G
• MyVariant Identifiers: chr1:g.168014375C>G (hg19) ; chr1:g.168045137C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168045137C>G , CM000663.2:g.168045137C>G	GRCh38
NC_000001.10:g.168014375C>G , CM000663.1:g.168014375C>G	GRCh37
NC_000001.9:g.166280999C>G	NCBI36
NG_053062.1:g.113899C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367840.4:c.2168C>G MANE Select	ENSP00000356814.3:p.Thr723Ser
ENST00000312263.10:c.1937C>G	ENSP00000311949.6:p.Thr646Ser
ENST00000367840.3:c.2168C>G	ENSP00000356814.3:p.Thr723Ser
ENST00000367843.7:c.1997C>G	ENSP00000356817.3:p.Thr666Ser
ENST00000432587.6:c.2075C>G	ENSP00000396238.2:p.Thr692Ser
ENST00000478668.1:n.57C>G
ENST00000489398.1:n.736C>G
NM_001017977.2:c.1937C>G	NP_001017977.1:p.Thr646Ser
NM_001198956.1:c.2168C>G	NP_001185885.1:p.Thr723Ser
NM_001198957.1:c.2075C>G	NP_001185886.1:p.Thr692Ser
NM_018442.3:c.1997C>G	NP_060912.2:p.Thr666Ser
XM_005245331.3:c.2168C>G	XP_005245388.1:p.Thr723Ser
XM_005245332.3:c.1997C>G	XP_005245389.1:p.Thr666Ser
XM_005245333.3:c.1937C>G	XP_005245390.1:p.Thr646Ser
XM_011509767.1:c.1727C>G	XP_011508069.1:p.Thr576Ser
XR_921892.1:n.2261C>G
XR_921893.1:n.2090C>G
NM_001349773.1:c.2168C>G	NP_001336702.1:p.Thr723Ser
NM_001349774.1:c.1556C>G	NP_001336703.1:p.Thr519Ser
NM_001349775.1:c.1556C>G	NP_001336704.1:p.Thr519Ser
NM_001349776.1:c.1556C>G	NP_001336705.1:p.Thr519Ser
NM_001349777.1:c.1556C>G	NP_001336706.1:p.Thr519Ser
NM_001349778.1:c.1496C>G	NP_001336707.1:p.Thr499Ser
NM_001349779.1:c.1496C>G	NP_001336708.1:p.Thr499Ser
NM_001349780.1:c.1496C>G	NP_001336709.1:p.Thr499Ser
NR_146228.1:n.1856C>G
NR_146229.1:n.2473C>G
NR_146230.1:n.2172C>G
XM_005245332.5:c.1997C>G	XP_005245389.1:p.Thr666Ser
XM_005245333.5:c.1937C>G	XP_005245390.1:p.Thr646Ser
XM_017001779.2:c.1727C>G	XP_016857268.1:p.Thr576Ser
XM_024448371.1:c.1727C>G	XP_024304139.1:p.Thr576Ser
XM_024448372.1:c.1556C>G	XP_024304140.1:p.Thr519Ser
XM_024448373.1:c.1496C>G	XP_024304141.1:p.Thr499Ser
XM_024448374.1:c.1496C>G	XP_024304142.1:p.Thr499Ser
XM_024448375.1:c.1496C>G	XP_024304143.1:p.Thr499Ser
NM_001017977.3:c.1937C>G	NP_001017977.1:p.Thr646Ser
NM_001198956.2:c.2168C>G MANE Select	NP_001185885.1:p.Thr723Ser
NM_001198957.2:c.2075C>G	NP_001185886.1:p.Thr692Ser
NM_001349773.2:c.2168C>G	NP_001336702.1:p.Thr723Ser
NM_001349774.2:c.1556C>G	NP_001336703.1:p.Thr519Ser
NM_001349775.2:c.1556C>G	NP_001336704.1:p.Thr519Ser
NM_001349776.2:c.1556C>G	NP_001336705.1:p.Thr519Ser
NM_001349777.2:c.1556C>G	NP_001336706.1:p.Thr519Ser
NM_001349778.2:c.1496C>G	NP_001336707.1:p.Thr499Ser
NM_001349779.2:c.1496C>G	NP_001336708.1:p.Thr499Ser
NM_001349780.2:c.1496C>G	NP_001336709.1:p.Thr499Ser
NM_001393650.1:c.1937C>G	NP_001380579.1:p.Thr646Ser
NM_001393651.1:c.1997C>G	NP_001380580.1:p.Thr666Ser
NM_018442.4:c.1997C>G	NP_060912.2:p.Thr666Ser
NR_146228.2:n.1732C>G
NR_146229.2:n.2349C>G
NR_146230.2:n.2048C>G