Canonical Allele Identifier: CA2673260095
Gene: CTNND2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.11385170_11385171insAGC , CM000667.2:g.11385170_11385171insAGC GRCh38
NC_000005.9:g.11385282_11385283insAGC , CM000667.1:g.11385282_11385283insAGC GRCh37
NC_000005.8:g.11438282_11438283insAGC NCBI36
NG_023544.1:g.523830_523831insTGC
NG_023544.2:g.523830_523831insTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000706271.1:c.167-20279_167-20278insTGC ENSP00000516315.1:n.167-20279_167-20278insTGC
ENST00000304623.13:c.673_674insTGC MANE Select ENSP00000307134.8:p.Pro224_Pro225insLeu
ENST00000304623.12:c.673_674insTGC ENSP00000307134.8:p.Pro224_Pro225insLeu
ENST00000502551.5:c.398-20279_398-20278insTGC ENSP00000422389.1:n.398-20279_398-20278insTGC
ENST00000503622.5:c.167-20279_167-20278insTGC ENSP00000426887.1:n.167-20279_167-20278insTGC
ENST00000504354.5:n.217-20279_217-20278insTGC
ENST00000504499.5:c.612+11862_612+11863insTGC ENSP00000421000.1:n.612+11862_612+11863insTGC
ENST00000511278.5:n.542-20279_542-20278insTGC
ENST00000511377.5:c.400_401insTGC ENSP00000426510.1:p.Pro133_Pro134insLeu
ENST00000513588.5:c.440-20279_440-20278insTGC ENSP00000421093.1:n.440-20279_440-20278insTGC
ENST00000513598.5:c.400_401insTGC ENSP00000426625.1:p.Pro133_Pro134insLeu
ENST00000514132.1:n.322_323insTGC
NM_001288715.1:c.400_401insTGC NP_001275644.1:p.Pro133_Pro134insLeu
NM_001288716.1:c.167-20279_167-20278insTGC NP_001275645.1:n.167-20279_167-20278insTGC
NM_001288717.1:c.-123+11862_-123+11863insTGC NP_001275646.1:n.-123+11862_-123+11863insTGC
NM_001332.3:c.673_674insTGC NP_001323.1:p.Pro224_Pro225insLeu
NR_109988.1:n.630-20279_630-20278insTGC
XM_005248251.2:c.673_674insTGC XP_005248308.1:p.Pro224_Pro225insLeu
XM_005248252.1:c.631_632insTGC XP_005248309.1:p.Pro210_Pro211insLeu
XM_005248253.1:c.400_401insTGC XP_005248310.1:p.Pro133_Pro134insLeu
XM_011513967.1:c.400_401insTGC XP_011512269.1:p.Pro133_Pro134insLeu
NM_001364128.1:c.167-20279_167-20278insTGC NP_001351057.1:n.167-20279_167-20278insTGC
XM_005248251.3:c.673_674insTGC XP_005248308.1:p.Pro224_Pro225insLeu
XM_005248252.2:c.631_632insTGC XP_005248309.1:p.Pro210_Pro211insLeu
XM_011513967.2:c.400_401insTGC XP_011512269.1:p.Pro133_Pro134insLeu
XM_017009072.1:c.440-20279_440-20278insTGC XP_016864561.1:n.440-20279_440-20278insTGC
XM_017009073.1:c.398-20279_398-20278insTGC XP_016864562.1:n.398-20279_398-20278insTGC
XM_017009074.1:c.440-20279_440-20278insTGC XP_016864563.1:n.440-20279_440-20278insTGC
XM_017009075.2:c.167-20279_167-20278insTGC XP_016864564.1:n.167-20279_167-20278insTGC
NM_001332.4:c.673_674insTGC MANE Select NP_001323.1:p.Pro224_Pro225insLeu
NM_001288717.2:c.-123+11862_-123+11863insTGC NP_001275646.1:n.-123+11862_-123+11863insTGC
NR_109988.2:n.1033-20279_1033-20278insTGC
NM_001364128.2:c.167-20279_167-20278insTGC NP_001351057.1:n.167-20279_167-20278insTGC