Canonical Allele Identifier: CA2580076036

Gene: CUX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.102189853del , CM000669.2:g.102189853del	GRCh38
NC_000007.13:g.101833133del , CM000669.1:g.101833133del	GRCh37
NC_000007.12:g.101619853del	NCBI36
NG_029476.2:g.378950del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292535.12:c.1058del MANE Select	ENSP00000292535.7:p.Glu353GlyfsTer2
ENST00000292538.9:c.1091del	ENSP00000292538.4:p.Glu364GlyfsTer2
ENST00000437600.9:c.1085del	ENSP00000414091.5:p.Glu362GlyfsTer2
ENST00000546411.7:c.1058del	ENSP00000450125.3:p.Glu353GlyfsTer2
ENST00000622516.6:c.1091del MANE Plus Clinical	ENSP00000484760.2:p.Glu364GlyfsTer2
ENST00000645010.1:c.1091del	ENSP00000496653.1:p.Glu364GlyfsTer2
ENST00000646649.1:c.1091del	ENSP00000494610.1:p.Glu364GlyfsTer2
ENST00000292535.11:c.1058del	ENSP00000292535.7:p.Glu353GlyfsTer2
ENST00000292538.8:c.1091del	ENSP00000292538.4:p.Glu364GlyfsTer2
ENST00000360264.7:c.1091del	ENSP00000353401.3:p.Glu364GlyfsTer2
ENST00000393824.7:c.974del	ENSP00000377410.3:p.Glu325GlyfsTer2
ENST00000425244.6:c.953del	ENSP00000409745.2:p.Glu318GlyfsTer2
ENST00000437600.8:c.1091del	ENSP00000414091.4:p.Glu364GlyfsTer2
ENST00000546411.6:c.1058del	ENSP00000450125.2:p.Glu353GlyfsTer2
ENST00000547394.6:c.1043del	ENSP00000449371.2:p.Glu348GlyfsTer2
ENST00000549414.6:c.1058del	ENSP00000446630.2:p.Glu353GlyfsTer2
ENST00000550008.6:c.1058del	ENSP00000447373.2:p.Glu353GlyfsTer2
ENST00000556210.1:c.1058del	ENSP00000451558.1:p.Glu353GlyfsTer2
ENST00000558836.5:n.1197del
ENST00000560541.5:n.1363del
ENST00000622516.4:c.1085del	ENSP00000484760.1:p.Glu362GlyfsTer2
NM_001202543.1:c.1091del	NP_001189472.1:p.Glu364GlyfsTer2
NM_001202544.2:c.1043del	NP_001189473.1:p.Glu348GlyfsTer2
NM_001202545.2:c.953del	NP_001189474.1:p.Glu318GlyfsTer2
NM_001202546.2:c.974del	NP_001189475.1:p.Glu325GlyfsTer2
NM_001913.4:c.1091del	NP_001904.2:p.Glu364GlyfsTer2
NM_181500.3:c.1085del	NP_852477.1:p.Glu362GlyfsTer2
NM_181552.3:c.1058del	NP_853530.2:p.Glu353GlyfsTer2
XM_005250150.1:c.1358del	XP_005250207.1:p.Glu453GlyfsTer2
XM_005250151.1:c.1352del	XP_005250208.1:p.Glu451GlyfsTer2
XM_005250154.3:c.1358del	XP_005250211.1:p.Glu453GlyfsTer2
XM_006715854.1:c.1358del	XP_006715917.1:p.Glu453GlyfsTer2
XM_006715855.1:c.1352del	XP_006715918.1:p.Glu451GlyfsTer2
XM_006715856.2:c.1091del	XP_006715919.1:p.Glu364GlyfsTer2
XM_011515823.1:c.1358del	XP_011514125.1:p.Glu453GlyfsTer2
XM_011515824.1:c.1352del	XP_011514126.1:p.Glu451GlyfsTer2
XM_011515825.1:c.1091del	XP_011514127.1:p.Glu364GlyfsTer2
XM_005250150.3:c.1358del	XP_005250207.1:p.Glu453GlyfsTer2
XM_006715854.2:c.1358del	XP_006715917.1:p.Glu453GlyfsTer2
XM_011515825.2:c.1091del	XP_011514127.1:p.Glu364GlyfsTer2
XM_017011760.2:c.1085del	XP_016867249.1:p.Glu362GlyfsTer2
XM_024446668.1:c.1352del	XP_024302436.1:p.Glu451GlyfsTer2
NM_181552.4:c.1058del MANE Select	NP_853530.2:p.Glu353GlyfsTer2
NM_001202543.2:c.1091del	NP_001189472.1:p.Glu364GlyfsTer2
NM_001202544.3:c.1043del	NP_001189473.1:p.Glu348GlyfsTer2
NM_001202545.3:c.953del	NP_001189474.1:p.Glu318GlyfsTer2
NM_001202546.3:c.974del	NP_001189475.1:p.Glu325GlyfsTer2
NM_001913.5:c.1091del MANE Plus Clinical	NP_001904.2:p.Glu364GlyfsTer2
NM_181500.4:c.1085del	NP_852477.1:p.Glu362GlyfsTer2