Canonical Allele Identifier: CA390187784

Gene: DCAF5

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.69054729T>C , CM000676.2:g.69054729T>C	GRCh38
NC_000014.8:g.69521446T>C , CM000676.1:g.69521446T>C	GRCh37
NC_000014.7:g.68591199T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341516.10:c.1957A>G MANE Select	ENSP00000341351.5:p.Ile653Val
ENST00000341516.9:c.1957A>G	ENSP00000341351.5:p.Ile653Val
ENST00000554215.5:c.1711A>G	ENSP00000451551.1:p.Ile571Val
ENST00000556847.5:c.1711A>G	ENSP00000452052.1:p.Ile571Val
ENST00000557386.5:c.1954A>G	ENSP00000451845.1:p.Ile652Val
NM_001284206.1:c.1954A>G	NP_001271135.1:p.Ile652Val
NM_001284207.1:c.1711A>G	NP_001271136.1:p.Ile571Val
NM_003861.2:c.1957A>G	NP_003852.1:p.Ile653Val
XM_005268164.3:c.931A>G	XP_005268221.1:p.Ile311Val
XM_006720297.2:c.2062A>G	XP_006720360.1:p.Ile688Val
XM_006720298.2:c.2059A>G	XP_006720361.1:p.Ile687Val
XM_006720299.2:c.1816A>G	XP_006720362.1:p.Ile606Val
XM_006720300.2:c.1813A>G	XP_006720363.1:p.Ile605Val
XM_011537278.1:c.1816A>G	XP_011535580.1:p.Ile606Val
XM_011537279.1:c.1816A>G	XP_011535581.1:p.Ile606Val
XM_011537280.1:c.1411A>G	XP_011535582.1:p.Ile471Val
XM_011537281.1:c.931A>G	XP_011535583.1:p.Ile311Val
XM_006720299.3:c.1816A>G	XP_006720362.1:p.Ile606Val
XM_011537279.2:c.1816A>G	XP_011535581.1:p.Ile606Val
XM_011537280.3:c.1411A>G	XP_011535582.1:p.Ile471Val
XM_017021733.1:c.1816A>G	XP_016877222.1:p.Ile606Val
XM_017021734.1:c.1711A>G	XP_016877223.1:p.Ile571Val
XM_017021735.1:c.1711A>G	XP_016877224.1:p.Ile571Val
XM_017021736.1:c.1708A>G	XP_016877225.1:p.Ile570Val
XM_017021737.1:c.1306A>G	XP_016877226.1:p.Ile436Val
XM_017021738.1:c.1120A>G	XP_016877227.1:p.Ile374Val
XM_017021739.1:c.1120A>G	XP_016877228.1:p.Ile374Val
NM_003861.3:c.1957A>G MANE Select	NP_003852.1:p.Ile653Val