Canonical Allele Identifier: CA2580076043
Gene: CUX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.102202166del , CM000669.2:g.102202166del GRCh38
NC_000007.13:g.101845446del , CM000669.1:g.101845446del GRCh37
NC_000007.12:g.101632166del NCBI36
NG_029476.2:g.391263del

Transcript Alleles

HGVS Amino-acid Change
ENST00000292535.12:c.2869del MANE Select ENSP00000292535.7:p.Ala957ProfsTer?
ENST00000292538.9:c.1255+6563del ENSP00000292538.4:n.1255+6563del
ENST00000437600.9:c.1249+6563del ENSP00000414091.5:n.1249+6563del
ENST00000546411.7:c.2869del ENSP00000450125.3:p.Ala957ProfsTer?
ENST00000622516.6:c.1255+6563del MANE Plus Clinical ENSP00000484760.2:n.1255+6563del
ENST00000645010.1:c.2734del ENSP00000496653.1:p.Ala912ProfsTer?
ENST00000646649.1:c.2428del ENSP00000494610.1:p.Ala810ProfsTer?
ENST00000292535.11:c.2869del ENSP00000292535.7:p.Ala957ProfsTer?
ENST00000292538.8:c.1255+6563del ENSP00000292538.4:n.1255+6563del
ENST00000360264.7:c.2902del ENSP00000353401.3:p.Ala968ProfsTer?
ENST00000393824.7:c.1138+6563del ENSP00000377410.3:n.1138+6563del
ENST00000425244.6:c.1117+6563del ENSP00000409745.2:n.1117+6563del
ENST00000437600.8:c.1255+6563del ENSP00000414091.4:n.1255+6563del
ENST00000546411.6:c.2563del ENSP00000450125.2:p.Ala855ProfsTer?
ENST00000547394.6:c.1207+6563del ENSP00000449371.2:n.1207+6563del
ENST00000549414.6:c.2803del ENSP00000446630.2:p.Ala935ProfsTer?
ENST00000550008.6:c.2701del ENSP00000447373.2:p.Ala901ProfsTer?
ENST00000556210.1:c.2395del ENSP00000451558.1:p.Ala799ProfsTer?
ENST00000558836.5:n.1361+6563del
ENST00000560541.5:n.1527+6563del
ENST00000622516.4:c.1249+6563del ENSP00000484760.1:n.1249+6563del
NM_001202543.1:c.2902del NP_001189472.1:p.Ala968ProfsTer?
NM_001202544.2:c.1207+6563del NP_001189473.1:n.1207+6563del
NM_001202545.2:c.1117+6563del NP_001189474.1:n.1117+6563del
NM_001202546.2:c.1138+6563del NP_001189475.1:n.1138+6563del
NM_001913.4:c.1255+6563del NP_001904.2:n.1255+6563del
NM_181500.3:c.1249+6563del NP_852477.1:n.1249+6563del
NM_181552.3:c.2869del NP_853530.2:p.Ala957ProfsTer?
XM_005250150.1:c.3166del XP_005250207.1:p.Ala1056ProfsTer?
XM_005250151.1:c.3163del XP_005250208.1:p.Ala1055ProfsTer?
XM_005250154.3:c.1522+6563del XP_005250211.1:n.1522+6563del
XM_006715854.1:c.3103del XP_006715917.1:p.Ala1035ProfsTer?
XM_006715855.1:c.1516+6563del XP_006715918.1:n.1516+6563del
XM_006715856.2:c.2836del XP_006715919.1:p.Ala946ProfsTer?
XM_011515823.1:c.2863del XP_011514125.1:p.Ala955ProfsTer?
XM_011515824.1:c.2857del XP_011514126.1:p.Ala953ProfsTer?
XM_011515825.1:c.2596del XP_011514127.1:p.Ala866ProfsTer?
XM_005250150.3:c.3166del XP_005250207.1:p.Ala1056ProfsTer?
XM_006715854.2:c.3103del XP_006715917.1:p.Ala1035ProfsTer?
XM_011515825.2:c.2596del XP_011514127.1:p.Ala866ProfsTer?
XM_017011760.2:c.2830del XP_016867249.1:p.Ala944ProfsTer?
XM_024446668.1:c.2857del XP_024302436.1:p.Ala953ProfsTer?
NM_181552.4:c.2869del MANE Select NP_853530.2:p.Ala957ProfsTer?
NM_001202543.2:c.2902del NP_001189472.1:p.Ala968ProfsTer?
NM_001202544.3:c.1207+6563del NP_001189473.1:n.1207+6563del
NM_001202545.3:c.1117+6563del NP_001189474.1:n.1117+6563del
NM_001202546.3:c.1138+6563del NP_001189475.1:n.1138+6563del
NM_001913.5:c.1255+6563del MANE Plus Clinical NP_001904.2:n.1255+6563del
NM_181500.4:c.1249+6563del NP_852477.1:n.1249+6563del