Canonical Allele Identifier: CA368685552
Gene: CUX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.102202103G>A , CM000669.2:g.102202103G>A GRCh38
NC_000007.13:g.101845383G>A , CM000669.1:g.101845383G>A GRCh37
NC_000007.12:g.101632103G>A NCBI36
NG_029476.2:g.391200G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000292535.12:c.2806G>A MANE Select ENSP00000292535.7:p.Glu936Lys
ENST00000292538.9:c.1255+6500G>A ENSP00000292538.4:n.1255+6500G>A
ENST00000437600.9:c.1249+6500G>A ENSP00000414091.5:n.1249+6500G>A
ENST00000546411.7:c.2806G>A ENSP00000450125.3:p.Glu936Lys
ENST00000622516.6:c.1255+6500G>A MANE Plus Clinical ENSP00000484760.2:n.1255+6500G>A
ENST00000645010.1:c.2671G>A ENSP00000496653.1:p.Glu891Lys
ENST00000646649.1:c.2365G>A ENSP00000494610.1:p.Glu789Lys
ENST00000292535.11:c.2806G>A ENSP00000292535.7:p.Glu936Lys
ENST00000292538.8:c.1255+6500G>A ENSP00000292538.4:n.1255+6500G>A
ENST00000360264.7:c.2839G>A ENSP00000353401.3:p.Glu947Lys
ENST00000393824.7:c.1138+6500G>A ENSP00000377410.3:n.1138+6500G>A
ENST00000425244.6:c.1117+6500G>A ENSP00000409745.2:n.1117+6500G>A
ENST00000437600.8:c.1255+6500G>A ENSP00000414091.4:n.1255+6500G>A
ENST00000546411.6:c.2500G>A ENSP00000450125.2:p.Glu834Lys
ENST00000547394.6:c.1207+6500G>A ENSP00000449371.2:n.1207+6500G>A
ENST00000549414.6:c.2740G>A ENSP00000446630.2:p.Glu914Lys
ENST00000550008.6:c.2638G>A ENSP00000447373.2:p.Glu880Lys
ENST00000556210.1:c.2332G>A ENSP00000451558.1:p.Glu778Lys
ENST00000558836.5:n.1361+6500G>A
ENST00000560541.5:n.1527+6500G>A
ENST00000622516.4:c.1249+6500G>A ENSP00000484760.1:n.1249+6500G>A
NM_001202543.1:c.2839G>A NP_001189472.1:p.Glu947Lys
NM_001202544.2:c.1207+6500G>A NP_001189473.1:n.1207+6500G>A
NM_001202545.2:c.1117+6500G>A NP_001189474.1:n.1117+6500G>A
NM_001202546.2:c.1138+6500G>A NP_001189475.1:n.1138+6500G>A
NM_001913.4:c.1255+6500G>A NP_001904.2:n.1255+6500G>A
NM_181500.3:c.1249+6500G>A NP_852477.1:n.1249+6500G>A
NM_181552.3:c.2806G>A NP_853530.2:p.Glu936Lys
XM_005250150.1:c.3103G>A XP_005250207.1:p.Glu1035Lys
XM_005250151.1:c.3100G>A XP_005250208.1:p.Glu1034Lys
XM_005250154.3:c.1522+6500G>A XP_005250211.1:n.1522+6500G>A
XM_006715854.1:c.3040G>A XP_006715917.1:p.Glu1014Lys
XM_006715855.1:c.1516+6500G>A XP_006715918.1:n.1516+6500G>A
XM_006715856.2:c.2773G>A XP_006715919.1:p.Glu925Lys
XM_011515823.1:c.2800G>A XP_011514125.1:p.Glu934Lys
XM_011515824.1:c.2794G>A XP_011514126.1:p.Glu932Lys
XM_011515825.1:c.2533G>A XP_011514127.1:p.Glu845Lys
XM_005250150.3:c.3103G>A XP_005250207.1:p.Glu1035Lys
XM_006715854.2:c.3040G>A XP_006715917.1:p.Glu1014Lys
XM_011515825.2:c.2533G>A XP_011514127.1:p.Glu845Lys
XM_017011760.2:c.2767G>A XP_016867249.1:p.Glu923Lys
XM_024446668.1:c.2794G>A XP_024302436.1:p.Glu932Lys
NM_181552.4:c.2806G>A MANE Select NP_853530.2:p.Glu936Lys
NM_001202543.2:c.2839G>A NP_001189472.1:p.Glu947Lys
NM_001202544.3:c.1207+6500G>A NP_001189473.1:n.1207+6500G>A
NM_001202545.3:c.1117+6500G>A NP_001189474.1:n.1117+6500G>A
NM_001202546.3:c.1138+6500G>A NP_001189475.1:n.1138+6500G>A
NM_001913.5:c.1255+6500G>A MANE Plus Clinical NP_001904.2:n.1255+6500G>A
NM_181500.4:c.1249+6500G>A NP_852477.1:n.1249+6500G>A