Canonical Allele Identifier: CA13748621

Gene: CUX2

Linked Data

• dbSNP Id: rs3847953
• gnomAD v2: 12-111765464-C-T
• gnomAD v3: 12-111327660-C-T
• gnomAD v4: 12-111327660-C-T
• MyVariant Identifiers: chr12:g.111765464C>T (hg19) ; chr12:g.111327660C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111327660C>T , CM000674.2:g.111327660C>T	GRCh38
NC_000012.11:g.111765464C>T , CM000674.1:g.111765464C>T	GRCh37
NC_000012.10:g.110249847C>T	NCBI36
NG_023039.1:g.298637C>T
NG_023039.2:g.298637C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261726.11:c.2926+5080C>T MANE Select	ENSP00000261726.6:n.2926+5080C>T
ENST00000261726.10:c.2926+5080C>T	ENSP00000261726.6:n.2926+5080C>T
NM_015267.3:c.2926+5080C>T	NP_056082.2:n.2926+5080C>T
XM_011538061.1:c.3094+5080C>T	XP_011536363.1:n.3094+5080C>T
XM_011538062.1:c.2983+5080C>T	XP_011536364.1:n.2983+5080C>T
XM_011538063.1:c.2959+5080C>T	XP_011536365.1:n.2959+5080C>T
XM_011538064.1:c.2902+5080C>T	XP_011536366.1:n.2902+5080C>T
XM_011538065.1:c.2740+5080C>T	XP_011536367.1:n.2740+5080C>T
XM_011538066.1:c.2740+5080C>T	XP_011536368.1:n.2740+5080C>T
XM_011538067.1:c.2740+5080C>T	XP_011536369.1:n.2740+5080C>T
XM_011538068.1:c.2740+5080C>T	XP_011536370.1:n.2740+5080C>T
XM_011538069.1:c.2740+5080C>T	XP_011536371.1:n.2740+5080C>T
XM_011538070.1:c.2740+5080C>T	XP_011536372.1:n.2740+5080C>T
XM_011538071.1:c.2740+5080C>T	XP_011536373.1:n.2740+5080C>T
XM_011538072.1:c.2740+5080C>T	XP_011536374.1:n.2740+5080C>T
XM_011538061.3:c.3094+5080C>T	XP_011536363.1:n.3094+5080C>T
XM_011538063.3:c.2959+5080C>T	XP_011536365.1:n.2959+5080C>T
XM_011538069.2:c.2740+5080C>T	XP_011536371.1:n.2740+5080C>T
XM_011538070.2:c.2740+5080C>T	XP_011536372.1:n.2740+5080C>T
XM_017019080.1:c.2740+5080C>T	XP_016874569.1:n.2740+5080C>T
XM_017019081.1:c.2740+5080C>T	XP_016874570.1:n.2740+5080C>T
NM_015267.4:c.2926+5080C>T MANE Select	NP_056082.2:n.2926+5080C>T
NM_001370598.1:c.2740+5080C>T	NP_001357527.1:n.2740+5080C>T