Canonical Allele Identifier: CA368681503

Gene: CUX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.102201654A>G , CM000669.2:g.102201654A>G	GRCh38
NC_000007.13:g.101844934A>G , CM000669.1:g.101844934A>G	GRCh37
NC_000007.12:g.101631654A>G	NCBI36
NG_029476.2:g.390751A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292535.12:c.2357A>G MANE Select	ENSP00000292535.7:p.Lys786Arg
ENST00000292538.9:c.1255+6051A>G	ENSP00000292538.4:n.1255+6051A>G
ENST00000437600.9:c.1249+6051A>G	ENSP00000414091.5:n.1249+6051A>G
ENST00000546411.7:c.2357A>G	ENSP00000450125.3:p.Lys786Arg
ENST00000622516.6:c.1255+6051A>G MANE Plus Clinical	ENSP00000484760.2:n.1255+6051A>G
ENST00000645010.1:c.2222A>G	ENSP00000496653.1:p.Lys741Arg
ENST00000646649.1:c.1916A>G	ENSP00000494610.1:p.Lys639Arg
ENST00000292535.11:c.2357A>G	ENSP00000292535.7:p.Lys786Arg
ENST00000292538.8:c.1255+6051A>G	ENSP00000292538.4:n.1255+6051A>G
ENST00000360264.7:c.2390A>G	ENSP00000353401.3:p.Lys797Arg
ENST00000393824.7:c.1138+6051A>G	ENSP00000377410.3:n.1138+6051A>G
ENST00000425244.6:c.1117+6051A>G	ENSP00000409745.2:n.1117+6051A>G
ENST00000437600.8:c.1255+6051A>G	ENSP00000414091.4:n.1255+6051A>G
ENST00000546411.6:c.2051A>G	ENSP00000450125.2:p.Lys684Arg
ENST00000547394.6:c.1207+6051A>G	ENSP00000449371.2:n.1207+6051A>G
ENST00000549414.6:c.2291A>G	ENSP00000446630.2:p.Lys764Arg
ENST00000550008.6:c.2189A>G	ENSP00000447373.2:p.Lys730Arg
ENST00000556210.1:c.1883A>G	ENSP00000451558.1:p.Lys628Arg
ENST00000558836.5:n.1361+6051A>G
ENST00000560541.5:n.1527+6051A>G
ENST00000622516.4:c.1249+6051A>G	ENSP00000484760.1:n.1249+6051A>G
NM_001202543.1:c.2390A>G	NP_001189472.1:p.Lys797Arg
NM_001202544.2:c.1207+6051A>G	NP_001189473.1:n.1207+6051A>G
NM_001202545.2:c.1117+6051A>G	NP_001189474.1:n.1117+6051A>G
NM_001202546.2:c.1138+6051A>G	NP_001189475.1:n.1138+6051A>G
NM_001913.4:c.1255+6051A>G	NP_001904.2:n.1255+6051A>G
NM_181500.3:c.1249+6051A>G	NP_852477.1:n.1249+6051A>G
NM_181552.3:c.2357A>G	NP_853530.2:p.Lys786Arg
XM_005250150.1:c.2654A>G	XP_005250207.1:p.Lys885Arg
XM_005250151.1:c.2651A>G	XP_005250208.1:p.Lys884Arg
XM_005250154.3:c.1522+6051A>G	XP_005250211.1:n.1522+6051A>G
XM_006715854.1:c.2591A>G	XP_006715917.1:p.Lys864Arg
XM_006715855.1:c.1516+6051A>G	XP_006715918.1:n.1516+6051A>G
XM_006715856.2:c.2324A>G	XP_006715919.1:p.Lys775Arg
XM_011515823.1:c.2351A>G	XP_011514125.1:p.Lys784Arg
XM_011515824.1:c.2345A>G	XP_011514126.1:p.Lys782Arg
XM_011515825.1:c.2084A>G	XP_011514127.1:p.Lys695Arg
XM_005250150.3:c.2654A>G	XP_005250207.1:p.Lys885Arg
XM_006715854.2:c.2591A>G	XP_006715917.1:p.Lys864Arg
XM_011515825.2:c.2084A>G	XP_011514127.1:p.Lys695Arg
XM_017011760.2:c.2318A>G	XP_016867249.1:p.Lys773Arg
XM_024446668.1:c.2345A>G	XP_024302436.1:p.Lys782Arg
NM_181552.4:c.2357A>G MANE Select	NP_853530.2:p.Lys786Arg
NM_001202543.2:c.2390A>G	NP_001189472.1:p.Lys797Arg
NM_001202544.3:c.1207+6051A>G	NP_001189473.1:n.1207+6051A>G
NM_001202545.3:c.1117+6051A>G	NP_001189474.1:n.1117+6051A>G
NM_001202546.3:c.1138+6051A>G	NP_001189475.1:n.1138+6051A>G
NM_001913.5:c.1255+6051A>G MANE Plus Clinical	NP_001904.2:n.1255+6051A>G
NM_181500.4:c.1249+6051A>G	NP_852477.1:n.1249+6051A>G