Canonical Allele Identifier: CA368665500

Gene: CUX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.102239522A>C , CM000669.2:g.102239522A>C	GRCh38
NC_000007.13:g.101882802A>C , CM000669.1:g.101882802A>C	GRCh37
NC_000007.12:g.101669522A>C	NCBI36
NG_029476.2:g.428619A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292535.12:c.3825A>C MANE Select	ENSP00000292535.7:p.Glu1275Asp
ENST00000292538.9:c.1256-33844A>C	ENSP00000292538.4:n.1256-33844A>C
ENST00000437600.9:c.1250-33844A>C	ENSP00000414091.5:n.1250-33844A>C
ENST00000546411.7:c.3825A>C	ENSP00000450125.3:p.Glu1275Asp
ENST00000622516.6:c.1256-33844A>C MANE Plus Clinical	ENSP00000484760.2:n.1256-33844A>C
ENST00000645010.1:c.3690A>C	ENSP00000496653.1:p.Glu1230Asp
ENST00000646649.1:c.3384A>C	ENSP00000494610.1:p.Glu1128Asp
ENST00000292535.11:c.3825A>C	ENSP00000292535.7:p.Glu1275Asp
ENST00000292538.8:c.1256-33844A>C	ENSP00000292538.4:n.1256-33844A>C
ENST00000360264.7:c.3858A>C	ENSP00000353401.3:p.Glu1286Asp
ENST00000393824.7:c.1139-33844A>C	ENSP00000377410.3:n.1139-33844A>C
ENST00000425244.6:c.1118-33844A>C	ENSP00000409745.2:n.1118-33844A>C
ENST00000437600.8:c.1256-33844A>C	ENSP00000414091.4:n.1256-33844A>C
ENST00000546411.6:c.3519A>C	ENSP00000450125.2:p.Glu1173Asp
ENST00000547394.6:c.1208-33844A>C	ENSP00000449371.2:n.1208-33844A>C
ENST00000549414.6:c.3759A>C	ENSP00000446630.2:p.Glu1253Asp
ENST00000550008.6:c.3657A>C	ENSP00000447373.2:p.Glu1219Asp
ENST00000556210.1:c.3351A>C	ENSP00000451558.1:p.Glu1117Asp
ENST00000558836.5:n.1362-33844A>C
ENST00000560541.5:n.1528-33844A>C
ENST00000622516.4:c.1250-33844A>C	ENSP00000484760.1:n.1250-33844A>C
NM_001202543.1:c.3858A>C	NP_001189472.1:p.Glu1286Asp
NM_001202544.2:c.1208-33844A>C	NP_001189473.1:n.1208-33844A>C
NM_001202545.2:c.1118-33844A>C	NP_001189474.1:n.1118-33844A>C
NM_001202546.2:c.1139-33844A>C	NP_001189475.1:n.1139-33844A>C
NM_001913.4:c.1256-33844A>C	NP_001904.2:n.1256-33844A>C
NM_181500.3:c.1250-33844A>C	NP_852477.1:n.1250-33844A>C
NM_181552.3:c.3825A>C	NP_853530.2:p.Glu1275Asp
XM_005250150.1:c.4122A>C	XP_005250207.1:p.Glu1374Asp
XM_005250151.1:c.4119A>C	XP_005250208.1:p.Glu1373Asp
XM_005250154.3:c.1523-33844A>C	XP_005250211.1:n.1523-33844A>C
XM_006715854.1:c.4059A>C	XP_006715917.1:p.Glu1353Asp
XM_006715855.1:c.1517-33844A>C	XP_006715918.1:n.1517-33844A>C
XM_006715856.2:c.3792A>C	XP_006715919.1:p.Glu1264Asp
XM_011515823.1:c.3819A>C	XP_011514125.1:p.Glu1273Asp
XM_011515824.1:c.3813A>C	XP_011514126.1:p.Glu1271Asp
XM_011515825.1:c.3552A>C	XP_011514127.1:p.Glu1184Asp
XM_005250150.3:c.4122A>C	XP_005250207.1:p.Glu1374Asp
XM_006715854.2:c.4059A>C	XP_006715917.1:p.Glu1353Asp
XM_011515825.2:c.3552A>C	XP_011514127.1:p.Glu1184Asp
XM_017011760.2:c.3786A>C	XP_016867249.1:p.Glu1262Asp
XM_024446668.1:c.3813A>C	XP_024302436.1:p.Glu1271Asp
NM_181552.4:c.3825A>C MANE Select	NP_853530.2:p.Glu1275Asp
NM_001202543.2:c.3858A>C	NP_001189472.1:p.Glu1286Asp
NM_001202544.3:c.1208-33844A>C	NP_001189473.1:n.1208-33844A>C
NM_001202545.3:c.1118-33844A>C	NP_001189474.1:n.1118-33844A>C
NM_001202546.3:c.1139-33844A>C	NP_001189475.1:n.1139-33844A>C
NM_001913.5:c.1256-33844A>C MANE Plus Clinical	NP_001904.2:n.1256-33844A>C
NM_181500.4:c.1250-33844A>C	NP_852477.1:n.1250-33844A>C