Canonical Allele Identifier: CA2556568971
Gene: CTNND2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.11320263_11320264insAGAGTTACACAAAATATTGTATTTGAGCATCGATTTAATTTCCT , CM000667.2:g.11320263_11320264insAGAGTTACACAAAATATTGTATTTGAGCATCGATTTAATTTCCT GRCh38
NC_000005.9:g.11320375_11320376insAGAGTTACACAAAATATTGTATTTGAGCATCGATTTAATTTCCT , CM000667.1:g.11320375_11320376insAGAGTTACACAAAATATTGTATTTGAGCATCGATTTAATTTCCT GRCh37
NC_000005.8:g.11373375_11373376insAGAGTTACACAAAATATTGTATTTGAGCATCGATTTAATTTCCT NCBI36
NG_023544.1:g.588735_588736insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT
NG_023544.2:g.588735_588736insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000706271.1:c.617+26108_617+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT ENSP00000516315.1:n.617+26108_617+26109insAGGAAATTAAATCGATGCT...
ENST00000706272.1:c.700+26108_700+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT
ENST00000304623.13:c.1628+26108_1628+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT MANE Select ENSP00000307134.8:n.1628+26108_1628+26109insAGGAAATTAAATCGATG...
ENST00000304623.12:c.1628+26108_1628+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT ENSP00000307134.8:n.1628+26108_1628+26109insAGGAAATTAAATCGATG...
ENST00000495388.6:n.713+26108_713+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT
ENST00000503622.5:c.617+26108_617+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT ENSP00000426887.1:n.617+26108_617+26109insAGGAAATTAAATCGATGCT...
ENST00000504499.5:c.*367+26108_*367+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT ENSP00000421000.1:n.*367+26108_*367+26109insAGGAAATTAAATCGATG...
ENST00000511377.5:c.1355+26108_1355+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT ENSP00000426510.1:n.1355+26108_1355+26109insAGGAAATTAAATCGATG...
ENST00000513588.5:c.890+26108_890+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT ENSP00000421093.1:n.890+26108_890+26109insAGGAAATTAAATCGATGCT...
NM_001288715.1:c.1355+26108_1355+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT NP_001275644.1:n.1355+26108_1355+26109insAGGAAATTAAATCGATGCTC...
NM_001288716.1:c.617+26108_617+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT NP_001275645.1:n.617+26108_617+26109insAGGAAATTAAATCGATGCTCAA...
NM_001288717.1:c.329+26108_329+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT NP_001275646.1:n.329+26108_329+26109insAGGAAATTAAATCGATGCTCAA...
NM_001332.3:c.1628+26108_1628+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT NP_001323.1:n.1628+26108_1628+26109insAGGAAATTAAATCGATGCTCAAA...
NR_109988.1:n.1080+26108_1080+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT
XM_005248251.2:c.1628+26108_1628+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT XP_005248308.1:n.1628+26108_1628+26109insAGGAAATTAAATCGATGCTC...
XM_005248252.1:c.1586+26108_1586+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT XP_005248309.1:n.1586+26108_1586+26109insAGGAAATTAAATCGATGCTC...
XM_005248253.1:c.1355+26108_1355+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT XP_005248310.1:n.1355+26108_1355+26109insAGGAAATTAAATCGATGCTC...
XM_011513967.1:c.1355+26108_1355+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT XP_011512269.1:n.1355+26108_1355+26109insAGGAAATTAAATCGATGCTC...
NM_001364128.1:c.617+26108_617+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT NP_001351057.1:n.617+26108_617+26109insAGGAAATTAAATCGATGCTCAA...
XM_005248251.3:c.1628+26108_1628+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT XP_005248308.1:n.1628+26108_1628+26109insAGGAAATTAAATCGATGCTC...
XM_005248252.2:c.1586+26108_1586+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT XP_005248309.1:n.1586+26108_1586+26109insAGGAAATTAAATCGATGCTC...
XM_011513967.2:c.1355+26108_1355+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT XP_011512269.1:n.1355+26108_1355+26109insAGGAAATTAAATCGATGCTC...
XM_017009072.1:c.890+26108_890+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT XP_016864561.1:n.890+26108_890+26109insAGGAAATTAAATCGATGCTCAA...
XM_017009073.1:c.848+26108_848+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT XP_016864562.1:n.848+26108_848+26109insAGGAAATTAAATCGATGCTCAA...
XM_017009074.1:c.890+26108_890+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT XP_016864563.1:n.890+26108_890+26109insAGGAAATTAAATCGATGCTCAA...
XM_017009075.2:c.617+26108_617+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT XP_016864564.1:n.617+26108_617+26109insAGGAAATTAAATCGATGCTCAA...
XM_024454368.1:c.-44+44432_-44+44433insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT XP_024310136.1:n.-44+44432_-44+44433insAGGAAATTAAATCGATGCTCAA...
NM_001332.4:c.1628+26108_1628+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT MANE Select NP_001323.1:n.1628+26108_1628+26109insAGGAAATTAAATCGATGCTCAAA...
NM_001288717.2:c.329+26108_329+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT NP_001275646.1:n.329+26108_329+26109insAGGAAATTAAATCGATGCTCAA...
NR_109988.2:n.1483+26108_1483+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT
NM_001364128.2:c.617+26108_617+26109insAGGAAATTAAATCGATGCTCAAATACAATATTTTGTGTAACTCT NP_001351057.1:n.617+26108_617+26109insAGGAAATTAAATCGATGCTCAA...