Canonical Allele Identifier: CA163412454

Gene: CUX1

Linked Data

• dbSNP Id: rs551516494
• COSMIC: COSN21856768
• MyVariant Identifiers: chr7:g.101809765G>A (hg19) ; chr7:g.102166485G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.102166485G>A , CM000669.2:g.102166485G>A	GRCh38
NC_000007.13:g.101809765G>A , CM000669.1:g.101809765G>A	GRCh37
NC_000007.12:g.101596485G>A	NCBI36
NG_029476.2:g.355582G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000292535.12:c.724-3961G>A MANE Select	ENSP00000292535.7:n.724-3961G>A
ENST00000292538.9:c.757-3961G>A	ENSP00000292538.4:n.757-3961G>A
ENST00000437600.9:c.757-3961G>A	ENSP00000414091.5:n.757-3961G>A
ENST00000546411.7:c.724-3961G>A	ENSP00000450125.3:n.724-3961G>A
ENST00000622516.6:c.757-3961G>A MANE Plus Clinical	ENSP00000484760.2:n.757-3961G>A
ENST00000645010.1:c.757-3961G>A	ENSP00000496653.1:n.757-3961G>A
ENST00000646649.1:c.757-3961G>A	ENSP00000494610.1:n.757-3961G>A
ENST00000292535.11:c.724-3961G>A	ENSP00000292535.7:n.724-3961G>A
ENST00000292538.8:c.757-3961G>A	ENSP00000292538.4:n.757-3961G>A
ENST00000360264.7:c.757-3961G>A	ENSP00000353401.3:n.757-3961G>A
ENST00000393824.7:c.646-3961G>A	ENSP00000377410.3:n.646-3961G>A
ENST00000425244.6:c.619-3961G>A	ENSP00000409745.2:n.619-3961G>A
ENST00000437600.8:c.757-3961G>A	ENSP00000414091.4:n.757-3961G>A
ENST00000546411.6:c.724-3961G>A	ENSP00000450125.2:n.724-3961G>A
ENST00000547394.6:c.709-3961G>A	ENSP00000449371.2:n.709-3961G>A
ENST00000549414.6:c.724-3961G>A	ENSP00000446630.2:n.724-3961G>A
ENST00000550008.6:c.724-3961G>A	ENSP00000447373.2:n.724-3961G>A
ENST00000556210.1:c.724-3961G>A	ENSP00000451558.1:n.724-3961G>A
ENST00000558836.5:n.863-3961G>A
ENST00000560541.5:n.1029-3961G>A
ENST00000622516.4:c.757-3961G>A	ENSP00000484760.1:n.757-3961G>A
NM_001202543.1:c.757-3961G>A	NP_001189472.1:n.757-3961G>A
NM_001202544.2:c.709-3961G>A	NP_001189473.1:n.709-3961G>A
NM_001202545.2:c.619-3961G>A	NP_001189474.1:n.619-3961G>A
NM_001202546.2:c.646-3961G>A	NP_001189475.1:n.646-3961G>A
NM_001913.4:c.757-3961G>A	NP_001904.2:n.757-3961G>A
NM_181500.3:c.757-3961G>A	NP_852477.1:n.757-3961G>A
NM_181552.3:c.724-3961G>A	NP_853530.2:n.724-3961G>A
XM_005250150.1:c.1024-3961G>A	XP_005250207.1:n.1024-3961G>A
XM_005250151.1:c.1024-3961G>A	XP_005250208.1:n.1024-3961G>A
XM_005250154.3:c.1024-3961G>A	XP_005250211.1:n.1024-3961G>A
XM_006715854.1:c.1024-3961G>A	XP_006715917.1:n.1024-3961G>A
XM_006715855.1:c.1024-3961G>A	XP_006715918.1:n.1024-3961G>A
XM_006715856.2:c.757-3961G>A	XP_006715919.1:n.757-3961G>A
XM_011515823.1:c.1024-3961G>A	XP_011514125.1:n.1024-3961G>A
XM_011515824.1:c.1024-3961G>A	XP_011514126.1:n.1024-3961G>A
XM_011515825.1:c.757-3961G>A	XP_011514127.1:n.757-3961G>A
XM_005250150.3:c.1024-3961G>A	XP_005250207.1:n.1024-3961G>A
XM_006715854.2:c.1024-3961G>A	XP_006715917.1:n.1024-3961G>A
XM_011515825.2:c.757-3961G>A	XP_011514127.1:n.757-3961G>A
XM_017011760.2:c.757-3961G>A	XP_016867249.1:n.757-3961G>A
XM_024446668.1:c.1024-3961G>A	XP_024302436.1:n.1024-3961G>A
NM_181552.4:c.724-3961G>A MANE Select	NP_853530.2:n.724-3961G>A
NM_001202543.2:c.757-3961G>A	NP_001189472.1:n.757-3961G>A
NM_001202544.3:c.709-3961G>A	NP_001189473.1:n.709-3961G>A
NM_001202545.3:c.619-3961G>A	NP_001189474.1:n.619-3961G>A
NM_001202546.3:c.646-3961G>A	NP_001189475.1:n.646-3961G>A
NM_001913.5:c.757-3961G>A MANE Plus Clinical	NP_001904.2:n.757-3961G>A
NM_181500.4:c.757-3961G>A	NP_852477.1:n.757-3961G>A