Canonical Allele Identifier: CA368899975

Gene: CUX1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.101816094G>A , CM000669.2:g.101816094G>A	GRCh38
NC_000007.13:g.101459374G>A , CM000669.1:g.101459374G>A	GRCh37
NC_000007.12:g.101246094G>A	NCBI36
NG_029476.2:g.5191G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292538.9:c.63+1G>A	ENSP00000292538.4:n.63+1G>A
ENST00000437600.9:c.63+1G>A	ENSP00000414091.5:n.63+1G>A
ENST00000622516.6:c.63+1G>A MANE Plus Clinical	ENSP00000484760.2:n.63+1G>A
ENST00000645010.1:c.63+1G>A	ENSP00000496653.1:n.63+1G>A
ENST00000646649.1:c.63+1G>A	ENSP00000494610.1:n.63+1G>A
ENST00000292538.8:c.63+1G>A	ENSP00000292538.4:n.63+1G>A
ENST00000360264.7:c.63+1G>A	ENSP00000353401.3:n.63+1G>A
ENST00000393824.7:c.63+1G>A	ENSP00000377410.3:n.63+1G>A
ENST00000425244.6:c.63+1G>A	ENSP00000409745.2:n.63+1G>A
ENST00000437600.8:c.63+1G>A	ENSP00000414091.4:n.63+1G>A
ENST00000497815.5:n.134+1G>A
ENST00000547394.6:c.63+1G>A	ENSP00000449371.2:n.63+1G>A
ENST00000607092.1:n.86+1G>A
ENST00000622516.4:c.63+1G>A	ENSP00000484760.1:n.63+1G>A
NM_001202543.1:c.63+1G>A	NP_001189472.1:n.63+1G>A
NM_001202544.2:c.63+1G>A	NP_001189473.1:n.63+1G>A
NM_001202545.2:c.63+1G>A	NP_001189474.1:n.63+1G>A
NM_001202546.2:c.63+1G>A	NP_001189475.1:n.63+1G>A
NM_001913.4:c.63+1G>A	NP_001904.2:n.63+1G>A
NM_181500.3:c.63+1G>A	NP_852477.1:n.63+1G>A
XM_006715856.2:c.63+1G>A	XP_006715919.1:n.63+1G>A
XM_011515825.1:c.63+1G>A	XP_011514127.1:n.63+1G>A
XM_011515825.2:c.63+1G>A	XP_011514127.1:n.63+1G>A
XM_017011760.2:c.63+1G>A	XP_016867249.1:n.63+1G>A
NM_001202543.2:c.63+1G>A	NP_001189472.1:n.63+1G>A
NM_001202544.3:c.63+1G>A	NP_001189473.1:n.63+1G>A
NM_001202545.3:c.63+1G>A	NP_001189474.1:n.63+1G>A
NM_001202546.3:c.63+1G>A	NP_001189475.1:n.63+1G>A
NM_001913.5:c.63+1G>A MANE Plus Clinical	NP_001904.2:n.63+1G>A
NM_181500.4:c.63+1G>A	NP_852477.1:n.63+1G>A