Canonical Allele Identifier: CA2063241191

Gene: CUX2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111270563C= , CM000674.2:g.111270563C=	GRCh38
NC_000012.11:g.111708367C= , CM000674.1:g.111708367C=	GRCh37
NC_000012.10:g.110192750C=	NCBI36
NG_023039.1:g.241540C=
NG_023039.2:g.241540C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261726.11:c.301+6724C= MANE Select	ENSP00000261726.6:n.301+6724C=
ENST00000261726.10:c.301+6724C=	ENSP00000261726.6:n.301+6724C=
ENST00000397643.3:c.481+6724C=	ENSP00000380765.3:n.481+6724C=
ENST00000551604.2:n.471C=
NM_015267.3:c.301+6724C=	NP_056082.2:n.301+6724C=
XM_011538061.1:c.469+6724C=	XP_011536363.1:n.469+6724C=
XM_011538062.1:c.358+6724C=	XP_011536364.1:n.358+6724C=
XM_011538063.1:c.469+6724C=	XP_011536365.1:n.469+6724C=
XM_011538064.1:c.277+6724C=	XP_011536366.1:n.277+6724C=
XM_011538065.1:c.115+6724C=	XP_011536367.1:n.115+6724C=
XM_011538066.1:c.115+6724C=	XP_011536368.1:n.115+6724C=
XM_011538067.1:c.115+6724C=	XP_011536369.1:n.115+6724C=
XM_011538068.1:c.115+6724C=	XP_011536370.1:n.115+6724C=
XM_011538069.1:c.115+6724C=	XP_011536371.1:n.115+6724C=
XM_011538070.1:c.115+6724C=	XP_011536372.1:n.115+6724C=
XM_011538071.1:c.115+6724C=	XP_011536373.1:n.115+6724C=
XM_011538072.1:c.115+6724C=	XP_011536374.1:n.115+6724C=
XM_011538061.3:c.469+6724C=	XP_011536363.1:n.469+6724C=
XM_011538063.3:c.469+6724C=	XP_011536365.1:n.469+6724C=
XM_011538069.2:c.115+6724C=	XP_011536371.1:n.115+6724C=
XM_011538070.2:c.115+6724C=	XP_011536372.1:n.115+6724C=
XM_017019080.1:c.115+6724C=	XP_016874569.1:n.115+6724C=
XM_017019081.1:c.115+6724C=	XP_016874570.1:n.115+6724C=
NM_015267.4:c.301+6724C= MANE Select	NP_056082.2:n.301+6724C=
NM_001370598.1:c.115+6724C=	NP_001357527.1:n.115+6724C=