Canonical Allele Identifier: CA2063223839

Gene: CUX2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111327535G= , CM000674.2:g.111327535G=	GRCh38
NC_000012.11:g.111765339G= , CM000674.1:g.111765339G=	GRCh37
NC_000012.10:g.110249722G=	NCBI36
NG_023039.1:g.298512G=
NG_023039.2:g.298512G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261726.11:c.2926+4955G= MANE Select	ENSP00000261726.6:n.2926+4955G=
ENST00000261726.10:c.2926+4955G=	ENSP00000261726.6:n.2926+4955G=
NM_015267.3:c.2926+4955G=	NP_056082.2:n.2926+4955G=
XM_011538061.1:c.3094+4955G=	XP_011536363.1:n.3094+4955G=
XM_011538062.1:c.2983+4955G=	XP_011536364.1:n.2983+4955G=
XM_011538063.1:c.2959+4955G=	XP_011536365.1:n.2959+4955G=
XM_011538064.1:c.2902+4955G=	XP_011536366.1:n.2902+4955G=
XM_011538065.1:c.2740+4955G=	XP_011536367.1:n.2740+4955G=
XM_011538066.1:c.2740+4955G=	XP_011536368.1:n.2740+4955G=
XM_011538067.1:c.2740+4955G=	XP_011536369.1:n.2740+4955G=
XM_011538068.1:c.2740+4955G=	XP_011536370.1:n.2740+4955G=
XM_011538069.1:c.2740+4955G=	XP_011536371.1:n.2740+4955G=
XM_011538070.1:c.2740+4955G=	XP_011536372.1:n.2740+4955G=
XM_011538071.1:c.2740+4955G=	XP_011536373.1:n.2740+4955G=
XM_011538072.1:c.2740+4955G=	XP_011536374.1:n.2740+4955G=
XM_011538061.3:c.3094+4955G=	XP_011536363.1:n.3094+4955G=
XM_011538063.3:c.2959+4955G=	XP_011536365.1:n.2959+4955G=
XM_011538069.2:c.2740+4955G=	XP_011536371.1:n.2740+4955G=
XM_011538070.2:c.2740+4955G=	XP_011536372.1:n.2740+4955G=
XM_017019080.1:c.2740+4955G=	XP_016874569.1:n.2740+4955G=
XM_017019081.1:c.2740+4955G=	XP_016874570.1:n.2740+4955G=
NM_015267.4:c.2926+4955G= MANE Select	NP_056082.2:n.2926+4955G=
NM_001370598.1:c.2740+4955G=	NP_001357527.1:n.2740+4955G=