Canonical Allele Identifier: CA2497098238

Gene: CTNND2

Linked Data

• dbSNP Id: rs1363528910

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11320329_11320330dup , CM000667.2:g.11320329_11320330dup	GRCh38
NC_000005.9:g.11320441_11320442dup , CM000667.1:g.11320441_11320442dup	GRCh37
NC_000005.8:g.11373441_11373442dup	NCBI36
NG_023544.1:g.588675_588676dup
NG_023544.2:g.588675_588676dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000706271.1:c.617+26048_617+26049dup	ENSP00000516315.1:n.617+26048_617+26049du...
ENST00000706272.1:c.700+26048_700+26049dup
ENST00000304623.13:c.1628+26048_1628+26049dup MANE Select	ENSP00000307134.8:n.1628+26048_1628+26049...
ENST00000304623.12:c.1628+26048_1628+26049dup	ENSP00000307134.8:n.1628+26048_1628+26049...
ENST00000495388.6:n.713+26048_713+26049dup
ENST00000503622.5:c.617+26048_617+26049dup	ENSP00000426887.1:n.617+26048_617+26049du...
ENST00000504499.5:c.*367+26048_*367+26049dup	ENSP00000421000.1:n.*367+26048_*367+26049...
ENST00000511377.5:c.1355+26048_1355+26049dup	ENSP00000426510.1:n.1355+26048_1355+26049...
ENST00000513588.5:c.890+26048_890+26049dup	ENSP00000421093.1:n.890+26048_890+26049du...
NM_001288715.1:c.1355+26048_1355+26049dup	NP_001275644.1:n.1355+26048_1355+26049dup...
NM_001288716.1:c.617+26048_617+26049dup	NP_001275645.1:n.617+26048_617+26049dup
NM_001288717.1:c.329+26048_329+26049dup	NP_001275646.1:n.329+26048_329+26049dup
NM_001332.3:c.1628+26048_1628+26049dup	NP_001323.1:n.1628+26048_1628+26049dup
NR_109988.1:n.1080+26048_1080+26049dup
XM_005248251.2:c.1628+26048_1628+26049dup	XP_005248308.1:n.1628+26048_1628+26049dup...
XM_005248252.1:c.1586+26048_1586+26049dup	XP_005248309.1:n.1586+26048_1586+26049dup...
XM_005248253.1:c.1355+26048_1355+26049dup	XP_005248310.1:n.1355+26048_1355+26049dup...
XM_011513967.1:c.1355+26048_1355+26049dup	XP_011512269.1:n.1355+26048_1355+26049dup...
NM_001364128.1:c.617+26048_617+26049dup	NP_001351057.1:n.617+26048_617+26049dup
XM_005248251.3:c.1628+26048_1628+26049dup	XP_005248308.1:n.1628+26048_1628+26049dup...
XM_005248252.2:c.1586+26048_1586+26049dup	XP_005248309.1:n.1586+26048_1586+26049dup...
XM_011513967.2:c.1355+26048_1355+26049dup	XP_011512269.1:n.1355+26048_1355+26049dup...
XM_017009072.1:c.890+26048_890+26049dup	XP_016864561.1:n.890+26048_890+26049dup
XM_017009073.1:c.848+26048_848+26049dup	XP_016864562.1:n.848+26048_848+26049dup
XM_017009074.1:c.890+26048_890+26049dup	XP_016864563.1:n.890+26048_890+26049dup
XM_017009075.2:c.617+26048_617+26049dup	XP_016864564.1:n.617+26048_617+26049dup
XM_024454368.1:c.-44+44372_-44+44373dup	XP_024310136.1:n.-44+44372_-44+44373dup
NM_001332.4:c.1628+26048_1628+26049dup MANE Select	NP_001323.1:n.1628+26048_1628+26049dup
NM_001288717.2:c.329+26048_329+26049dup	NP_001275646.1:n.329+26048_329+26049dup
NR_109988.2:n.1483+26048_1483+26049dup
NM_001364128.2:c.617+26048_617+26049dup	NP_001351057.1:n.617+26048_617+26049dup