Canonical Allele Identifier: CA368685759

Gene: CUX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.102202122A>T , CM000669.2:g.102202122A>T	GRCh38
NC_000007.13:g.101845402A>T , CM000669.1:g.101845402A>T	GRCh37
NC_000007.12:g.101632122A>T	NCBI36
NG_029476.2:g.391219A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292535.12:c.2825A>T MANE Select	ENSP00000292535.7:p.Glu942Val
ENST00000292538.9:c.1255+6519A>T	ENSP00000292538.4:n.1255+6519A>T
ENST00000437600.9:c.1249+6519A>T	ENSP00000414091.5:n.1249+6519A>T
ENST00000546411.7:c.2825A>T	ENSP00000450125.3:p.Glu942Val
ENST00000622516.6:c.1255+6519A>T MANE Plus Clinical	ENSP00000484760.2:n.1255+6519A>T
ENST00000645010.1:c.2690A>T	ENSP00000496653.1:p.Glu897Val
ENST00000646649.1:c.2384A>T	ENSP00000494610.1:p.Glu795Val
ENST00000292535.11:c.2825A>T	ENSP00000292535.7:p.Glu942Val
ENST00000292538.8:c.1255+6519A>T	ENSP00000292538.4:n.1255+6519A>T
ENST00000360264.7:c.2858A>T	ENSP00000353401.3:p.Glu953Val
ENST00000393824.7:c.1138+6519A>T	ENSP00000377410.3:n.1138+6519A>T
ENST00000425244.6:c.1117+6519A>T	ENSP00000409745.2:n.1117+6519A>T
ENST00000437600.8:c.1255+6519A>T	ENSP00000414091.4:n.1255+6519A>T
ENST00000546411.6:c.2519A>T	ENSP00000450125.2:p.Glu840Val
ENST00000547394.6:c.1207+6519A>T	ENSP00000449371.2:n.1207+6519A>T
ENST00000549414.6:c.2759A>T	ENSP00000446630.2:p.Glu920Val
ENST00000550008.6:c.2657A>T	ENSP00000447373.2:p.Glu886Val
ENST00000556210.1:c.2351A>T	ENSP00000451558.1:p.Glu784Val
ENST00000558836.5:n.1361+6519A>T
ENST00000560541.5:n.1527+6519A>T
ENST00000622516.4:c.1249+6519A>T	ENSP00000484760.1:n.1249+6519A>T
NM_001202543.1:c.2858A>T	NP_001189472.1:p.Glu953Val
NM_001202544.2:c.1207+6519A>T	NP_001189473.1:n.1207+6519A>T
NM_001202545.2:c.1117+6519A>T	NP_001189474.1:n.1117+6519A>T
NM_001202546.2:c.1138+6519A>T	NP_001189475.1:n.1138+6519A>T
NM_001913.4:c.1255+6519A>T	NP_001904.2:n.1255+6519A>T
NM_181500.3:c.1249+6519A>T	NP_852477.1:n.1249+6519A>T
NM_181552.3:c.2825A>T	NP_853530.2:p.Glu942Val
XM_005250150.1:c.3122A>T	XP_005250207.1:p.Glu1041Val
XM_005250151.1:c.3119A>T	XP_005250208.1:p.Glu1040Val
XM_005250154.3:c.1522+6519A>T	XP_005250211.1:n.1522+6519A>T
XM_006715854.1:c.3059A>T	XP_006715917.1:p.Glu1020Val
XM_006715855.1:c.1516+6519A>T	XP_006715918.1:n.1516+6519A>T
XM_006715856.2:c.2792A>T	XP_006715919.1:p.Glu931Val
XM_011515823.1:c.2819A>T	XP_011514125.1:p.Glu940Val
XM_011515824.1:c.2813A>T	XP_011514126.1:p.Glu938Val
XM_011515825.1:c.2552A>T	XP_011514127.1:p.Glu851Val
XM_005250150.3:c.3122A>T	XP_005250207.1:p.Glu1041Val
XM_006715854.2:c.3059A>T	XP_006715917.1:p.Glu1020Val
XM_011515825.2:c.2552A>T	XP_011514127.1:p.Glu851Val
XM_017011760.2:c.2786A>T	XP_016867249.1:p.Glu929Val
XM_024446668.1:c.2813A>T	XP_024302436.1:p.Glu938Val
NM_181552.4:c.2825A>T MANE Select	NP_853530.2:p.Glu942Val
NM_001202543.2:c.2858A>T	NP_001189472.1:p.Glu953Val
NM_001202544.3:c.1207+6519A>T	NP_001189473.1:n.1207+6519A>T
NM_001202545.3:c.1117+6519A>T	NP_001189474.1:n.1117+6519A>T
NM_001202546.3:c.1138+6519A>T	NP_001189475.1:n.1138+6519A>T
NM_001913.5:c.1255+6519A>T MANE Plus Clinical	NP_001904.2:n.1255+6519A>T
NM_181500.4:c.1249+6519A>T	NP_852477.1:n.1249+6519A>T