Canonical Allele Identifier: CA802073224

Gene: CTNND2

Linked Data

• dbSNP Id: rs1420792942
• gnomAD v3: 5-11320432-C-CAT
• gnomAD v4: 5-11320432-C-CAT
• MyVariant Identifiers: chr5:g.11320544_11320545insAT (hg19) ; chr5:g.11320432_11320433insAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11320434_11320435dup , CM000667.2:g.11320434_11320435dup	GRCh38
NC_000005.9:g.11320546_11320547dup , CM000667.1:g.11320546_11320547dup	GRCh37
NC_000005.8:g.11373546_11373547dup	NCBI36
NG_023544.1:g.588565_588566dup
NG_023544.2:g.588565_588566dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000706271.1:c.617+25938_617+25939dup	ENSP00000516315.1:n.617+25938_617+25939du...
ENST00000706272.1:c.700+25938_700+25939dup
ENST00000304623.13:c.1628+25938_1628+25939dup MANE Select	ENSP00000307134.8:n.1628+25938_1628+25939...
ENST00000304623.12:c.1628+25938_1628+25939dup	ENSP00000307134.8:n.1628+25938_1628+25939...
ENST00000495388.6:n.713+25938_713+25939dup
ENST00000503622.5:c.617+25938_617+25939dup	ENSP00000426887.1:n.617+25938_617+25939du...
ENST00000504499.5:c.*367+25938_*367+25939dup	ENSP00000421000.1:n.*367+25938_*367+25939...
ENST00000511377.5:c.1355+25938_1355+25939dup	ENSP00000426510.1:n.1355+25938_1355+25939...
ENST00000513588.5:c.890+25938_890+25939dup	ENSP00000421093.1:n.890+25938_890+25939du...
NM_001288715.1:c.1355+25938_1355+25939dup	NP_001275644.1:n.1355+25938_1355+25939dup...
NM_001288716.1:c.617+25938_617+25939dup	NP_001275645.1:n.617+25938_617+25939dup
NM_001288717.1:c.329+25938_329+25939dup	NP_001275646.1:n.329+25938_329+25939dup
NM_001332.3:c.1628+25938_1628+25939dup	NP_001323.1:n.1628+25938_1628+25939dup
NR_109988.1:n.1080+25938_1080+25939dup
XM_005248251.2:c.1628+25938_1628+25939dup	XP_005248308.1:n.1628+25938_1628+25939dup...
XM_005248252.1:c.1586+25938_1586+25939dup	XP_005248309.1:n.1586+25938_1586+25939dup...
XM_005248253.1:c.1355+25938_1355+25939dup	XP_005248310.1:n.1355+25938_1355+25939dup...
XM_011513967.1:c.1355+25938_1355+25939dup	XP_011512269.1:n.1355+25938_1355+25939dup...
NM_001364128.1:c.617+25938_617+25939dup	NP_001351057.1:n.617+25938_617+25939dup
XM_005248251.3:c.1628+25938_1628+25939dup	XP_005248308.1:n.1628+25938_1628+25939dup...
XM_005248252.2:c.1586+25938_1586+25939dup	XP_005248309.1:n.1586+25938_1586+25939dup...
XM_011513967.2:c.1355+25938_1355+25939dup	XP_011512269.1:n.1355+25938_1355+25939dup...
XM_017009072.1:c.890+25938_890+25939dup	XP_016864561.1:n.890+25938_890+25939dup
XM_017009073.1:c.848+25938_848+25939dup	XP_016864562.1:n.848+25938_848+25939dup
XM_017009074.1:c.890+25938_890+25939dup	XP_016864563.1:n.890+25938_890+25939dup
XM_017009075.2:c.617+25938_617+25939dup	XP_016864564.1:n.617+25938_617+25939dup
XM_024454368.1:c.-44+44262_-44+44263dup	XP_024310136.1:n.-44+44262_-44+44263dup
NM_001332.4:c.1628+25938_1628+25939dup MANE Select	NP_001323.1:n.1628+25938_1628+25939dup
NM_001288717.2:c.329+25938_329+25939dup	NP_001275646.1:n.329+25938_329+25939dup
NR_109988.2:n.1483+25938_1483+25939dup
NM_001364128.2:c.617+25938_617+25939dup	NP_001351057.1:n.617+25938_617+25939dup