Canonical Allele Identifier: CA16042498
Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 372985
ClinVar RCV Id: RCV000413978
dbSNP Id: rs1057518120

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.11397173T>C , CM000667.2:g.11397173T>C GRCh38
NC_000005.9:g.11397285T>C , CM000667.1:g.11397285T>C GRCh37
NC_000005.8:g.11450285T>C NCBI36
NG_023544.1:g.511826A>G
NG_023544.2:g.511826A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000706271.1:c.166+14363A>G ENSP00000516315.1:n.166+14363A>G
ENST00000304623.13:c.470A>G MANE Select ENSP00000307134.8:p.Gln157Arg
ENST00000304623.12:c.470A>G ENSP00000307134.8:p.Gln157Arg
ENST00000502551.5:c.397+14363A>G ENSP00000422389.1:n.397+14363A>G
ENST00000503622.5:c.166+14363A>G ENSP00000426887.1:n.166+14363A>G
ENST00000504354.5:n.217-32283A>G
ENST00000504499.5:c.470A>G ENSP00000421000.1:p.Gln157Arg
ENST00000508761.1:c.428A>G ENSP00000424296.1:p.Gln143Arg
ENST00000511278.5:n.541+14363A>G
ENST00000511377.5:c.197A>G ENSP00000426510.1:p.Gln66Arg
ENST00000513588.5:c.439+14363A>G ENSP00000421093.1:n.439+14363A>G
ENST00000513598.5:c.197A>G ENSP00000426625.1:p.Gln66Arg
NM_001288715.1:c.197A>G NP_001275644.1:p.Gln66Arg
NM_001288716.1:c.166+14363A>G NP_001275645.1:n.166+14363A>G
NM_001288717.1:c.-265A>G NP_001275646.1:n.-265A>G
NM_001332.3:c.470A>G NP_001323.1:p.Gln157Arg
NR_109988.1:n.629+14363A>G
XM_005248251.2:c.470A>G XP_005248308.1:p.Gln157Arg
XM_005248252.1:c.428A>G XP_005248309.1:p.Gln143Arg
XM_005248253.1:c.197A>G XP_005248310.1:p.Gln66Arg
XM_011513967.1:c.197A>G XP_011512269.1:p.Gln66Arg
NM_001364128.1:c.166+14363A>G NP_001351057.1:n.166+14363A>G
XM_005248251.3:c.470A>G XP_005248308.1:p.Gln157Arg
XM_005248252.2:c.428A>G XP_005248309.1:p.Gln143Arg
XM_011513967.2:c.197A>G XP_011512269.1:p.Gln66Arg
XM_017009072.1:c.439+14363A>G XP_016864561.1:n.439+14363A>G
XM_017009073.1:c.397+14363A>G XP_016864562.1:n.397+14363A>G
XM_017009074.1:c.439+14363A>G XP_016864563.1:n.439+14363A>G
XM_017009075.2:c.166+14363A>G XP_016864564.1:n.166+14363A>G
NM_001332.4:c.470A>G MANE Select NP_001323.1:p.Gln157Arg
NM_001288717.2:c.-265A>G NP_001275646.1:n.-265A>G
NR_109988.2:n.1032+14363A>G
NM_001364128.2:c.166+14363A>G NP_001351057.1:n.166+14363A>G