Canonical Allele Identifier: CA2552126833

Gene: CTNND2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11320440_11320441insACCTGC , CM000667.2:g.11320440_11320441insACCTGC	GRCh38
NC_000005.9:g.11320552_11320553insACCTGC , CM000667.1:g.11320552_11320553insACCTGC	GRCh37
NC_000005.8:g.11373552_11373553insACCTGC	NCBI36
NG_023544.1:g.588558_588559insGCAGGT
NG_023544.2:g.588558_588559insGCAGGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000706271.1:c.617+25931_617+25932insGCAGGT	ENSP00000516315.1:n.617+25931_617+25932in...
ENST00000706272.1:c.700+25931_700+25932insGCAGGT
ENST00000304623.13:c.1628+25931_1628+25932insGCAGGT MANE Select	ENSP00000307134.8:n.1628+25931_1628+25932...
ENST00000304623.12:c.1628+25931_1628+25932insGCAGGT	ENSP00000307134.8:n.1628+25931_1628+25932...
ENST00000495388.6:n.713+25931_713+25932insGCAGGT
ENST00000503622.5:c.617+25931_617+25932insGCAGGT	ENSP00000426887.1:n.617+25931_617+25932in...
ENST00000504499.5:c.*367+25931_*367+25932insGCAGGT	ENSP00000421000.1:n.*367+25931_*367+25932...
ENST00000511377.5:c.1355+25931_1355+25932insGCAGGT	ENSP00000426510.1:n.1355+25931_1355+25932...
ENST00000513588.5:c.890+25931_890+25932insGCAGGT	ENSP00000421093.1:n.890+25931_890+25932in...
NM_001288715.1:c.1355+25931_1355+25932insGCAGGT	NP_001275644.1:n.1355+25931_1355+25932ins...
NM_001288716.1:c.617+25931_617+25932insGCAGGT	NP_001275645.1:n.617+25931_617+25932insGC...
NM_001288717.1:c.329+25931_329+25932insGCAGGT	NP_001275646.1:n.329+25931_329+25932insGC...
NM_001332.3:c.1628+25931_1628+25932insGCAGGT	NP_001323.1:n.1628+25931_1628+25932insGCA...
NR_109988.1:n.1080+25931_1080+25932insGCAGGT
XM_005248251.2:c.1628+25931_1628+25932insGCAGGT	XP_005248308.1:n.1628+25931_1628+25932ins...
XM_005248252.1:c.1586+25931_1586+25932insGCAGGT	XP_005248309.1:n.1586+25931_1586+25932ins...
XM_005248253.1:c.1355+25931_1355+25932insGCAGGT	XP_005248310.1:n.1355+25931_1355+25932ins...
XM_011513967.1:c.1355+25931_1355+25932insGCAGGT	XP_011512269.1:n.1355+25931_1355+25932ins...
NM_001364128.1:c.617+25931_617+25932insGCAGGT	NP_001351057.1:n.617+25931_617+25932insGC...
XM_005248251.3:c.1628+25931_1628+25932insGCAGGT	XP_005248308.1:n.1628+25931_1628+25932ins...
XM_005248252.2:c.1586+25931_1586+25932insGCAGGT	XP_005248309.1:n.1586+25931_1586+25932ins...
XM_011513967.2:c.1355+25931_1355+25932insGCAGGT	XP_011512269.1:n.1355+25931_1355+25932ins...
XM_017009072.1:c.890+25931_890+25932insGCAGGT	XP_016864561.1:n.890+25931_890+25932insGC...
XM_017009073.1:c.848+25931_848+25932insGCAGGT	XP_016864562.1:n.848+25931_848+25932insGC...
XM_017009074.1:c.890+25931_890+25932insGCAGGT	XP_016864563.1:n.890+25931_890+25932insGC...
XM_017009075.2:c.617+25931_617+25932insGCAGGT	XP_016864564.1:n.617+25931_617+25932insGC...
XM_024454368.1:c.-44+44255_-44+44256insGCAGGT	XP_024310136.1:n.-44+44255_-44+44256insGC...
NM_001332.4:c.1628+25931_1628+25932insGCAGGT MANE Select	NP_001323.1:n.1628+25931_1628+25932insGCA...
NM_001288717.2:c.329+25931_329+25932insGCAGGT	NP_001275646.1:n.329+25931_329+25932insGC...
NR_109988.2:n.1483+25931_1483+25932insGCAGGT
NM_001364128.2:c.617+25931_617+25932insGCAGGT	NP_001351057.1:n.617+25931_617+25932insGC...