Canonical Allele Identifier: CA2063223881

Gene: CUX2

Linked Data

• dbSNP Id: rs1887877999

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111327577T>C , CM000674.2:g.111327577T>C	GRCh38
NC_000012.11:g.111765381T>C , CM000674.1:g.111765381T>C	GRCh37
NC_000012.10:g.110249764T>C	NCBI36
NG_023039.1:g.298554T>C
NG_023039.2:g.298554T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261726.11:c.2926+4997T>C MANE Select	ENSP00000261726.6:n.2926+4997T>C
ENST00000261726.10:c.2926+4997T>C	ENSP00000261726.6:n.2926+4997T>C
NM_015267.3:c.2926+4997T>C	NP_056082.2:n.2926+4997T>C
XM_011538061.1:c.3094+4997T>C	XP_011536363.1:n.3094+4997T>C
XM_011538062.1:c.2983+4997T>C	XP_011536364.1:n.2983+4997T>C
XM_011538063.1:c.2959+4997T>C	XP_011536365.1:n.2959+4997T>C
XM_011538064.1:c.2902+4997T>C	XP_011536366.1:n.2902+4997T>C
XM_011538065.1:c.2740+4997T>C	XP_011536367.1:n.2740+4997T>C
XM_011538066.1:c.2740+4997T>C	XP_011536368.1:n.2740+4997T>C
XM_011538067.1:c.2740+4997T>C	XP_011536369.1:n.2740+4997T>C
XM_011538068.1:c.2740+4997T>C	XP_011536370.1:n.2740+4997T>C
XM_011538069.1:c.2740+4997T>C	XP_011536371.1:n.2740+4997T>C
XM_011538070.1:c.2740+4997T>C	XP_011536372.1:n.2740+4997T>C
XM_011538071.1:c.2740+4997T>C	XP_011536373.1:n.2740+4997T>C
XM_011538072.1:c.2740+4997T>C	XP_011536374.1:n.2740+4997T>C
XM_011538061.3:c.3094+4997T>C	XP_011536363.1:n.3094+4997T>C
XM_011538063.3:c.2959+4997T>C	XP_011536365.1:n.2959+4997T>C
XM_011538069.2:c.2740+4997T>C	XP_011536371.1:n.2740+4997T>C
XM_011538070.2:c.2740+4997T>C	XP_011536372.1:n.2740+4997T>C
XM_017019080.1:c.2740+4997T>C	XP_016874569.1:n.2740+4997T>C
XM_017019081.1:c.2740+4997T>C	XP_016874570.1:n.2740+4997T>C
NM_015267.4:c.2926+4997T>C MANE Select	NP_056082.2:n.2926+4997T>C
NM_001370598.1:c.2740+4997T>C	NP_001357527.1:n.2740+4997T>C