Canonical Allele Identifier: CA243577858

Gene: CUX2

Linked Data

• dbSNP Id: rs150280332
• gnomAD v2: 12-111699503-G-A
• gnomAD v3: 12-111261699-G-A
• gnomAD v4: 12-111261699-G-A
• MyVariant Identifiers: chr12:g.111699503G>A (hg19) ; chr12:g.111261699G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111261699G>A , CM000674.2:g.111261699G>A	GRCh38
NC_000012.11:g.111699503G>A , CM000674.1:g.111699503G>A	GRCh37
NC_000012.10:g.110183886G>A	NCBI36
NG_023039.1:g.232676G>A
NG_023039.2:g.232676G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261726.11:c.223-2062G>A MANE Select	ENSP00000261726.6:n.223-2062G>A
ENST00000261726.10:c.223-2062G>A	ENSP00000261726.6:n.223-2062G>A
ENST00000397643.3:c.403-2062G>A	ENSP00000380765.3:n.403-2062G>A
ENST00000551604.2:n.59-2062G>A
NM_015267.3:c.223-2062G>A	NP_056082.2:n.223-2062G>A
XM_011538061.1:c.391-2062G>A	XP_011536363.1:n.391-2062G>A
XM_011538062.1:c.280-2062G>A	XP_011536364.1:n.280-2062G>A
XM_011538063.1:c.391-2062G>A	XP_011536365.1:n.391-2062G>A
XM_011538064.1:c.199-2062G>A	XP_011536366.1:n.199-2062G>A
XM_011538065.1:c.37-2062G>A	XP_011536367.1:n.37-2062G>A
XM_011538066.1:c.37-2062G>A	XP_011536368.1:n.37-2062G>A
XM_011538067.1:c.37-2062G>A	XP_011536369.1:n.37-2062G>A
XM_011538068.1:c.37-2062G>A	XP_011536370.1:n.37-2062G>A
XM_011538069.1:c.37-2062G>A	XP_011536371.1:n.37-2062G>A
XM_011538070.1:c.37-2062G>A	XP_011536372.1:n.37-2062G>A
XM_011538071.1:c.37-2062G>A	XP_011536373.1:n.37-2062G>A
XM_011538072.1:c.37-2062G>A	XP_011536374.1:n.37-2062G>A
XM_011538061.3:c.391-2062G>A	XP_011536363.1:n.391-2062G>A
XM_011538063.3:c.391-2062G>A	XP_011536365.1:n.391-2062G>A
XM_011538069.2:c.37-2062G>A	XP_011536371.1:n.37-2062G>A
XM_011538070.2:c.37-2062G>A	XP_011536372.1:n.37-2062G>A
XM_017019080.1:c.37-2062G>A	XP_016874569.1:n.37-2062G>A
XM_017019081.1:c.37-2062G>A	XP_016874570.1:n.37-2062G>A
NM_015267.4:c.223-2062G>A MANE Select	NP_056082.2:n.223-2062G>A
NM_001370598.1:c.37-2062G>A	NP_001357527.1:n.37-2062G>A