Canonical Allele Identifier: CA2673260099

Gene: CTNND2

Linked Data

• gnomAD v4: 5-11385182-C-CGGT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11385184_11385185insTGG , CM000667.2:g.11385184_11385185insTGG	GRCh38
NC_000005.9:g.11385296_11385297insTGG , CM000667.1:g.11385296_11385297insTGG	GRCh37
NC_000005.8:g.11438296_11438297insTGG	NCBI36
NG_023544.1:g.523816_523817insACC
NG_023544.2:g.523816_523817insACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-20293_167-20292insACC	ENSP00000516315.1:n.167-20293_167-20292insACC
ENST00000304623.13:c.659_660insACC MANE Select	ENSP00000307134.8:p.Pro220_Pro221insPro
ENST00000304623.12:c.659_660insACC	ENSP00000307134.8:p.Pro220_Pro221insPro
ENST00000502551.5:c.398-20293_398-20292insACC	ENSP00000422389.1:n.398-20293_398-20292insACC
ENST00000503622.5:c.167-20293_167-20292insACC	ENSP00000426887.1:n.167-20293_167-20292insACC
ENST00000504354.5:n.217-20293_217-20292insACC
ENST00000504499.5:c.612+11848_612+11849insACC	ENSP00000421000.1:n.612+11848_612+11849insACC
ENST00000511278.5:n.542-20293_542-20292insACC
ENST00000511377.5:c.386_387insACC	ENSP00000426510.1:p.Pro129_Pro130insPro
ENST00000513588.5:c.440-20293_440-20292insACC	ENSP00000421093.1:n.440-20293_440-20292insACC
ENST00000513598.5:c.386_387insACC	ENSP00000426625.1:p.Pro129_Pro130insPro
ENST00000514132.1:n.308_309insACC
NM_001288715.1:c.386_387insACC	NP_001275644.1:p.Pro129_Pro130insPro
NM_001288716.1:c.167-20293_167-20292insACC	NP_001275645.1:n.167-20293_167-20292insACC
NM_001288717.1:c.-123+11848_-123+11849insACC	NP_001275646.1:n.-123+11848_-123+11849insACC
NM_001332.3:c.659_660insACC	NP_001323.1:p.Pro220_Pro221insPro
NR_109988.1:n.630-20293_630-20292insACC
XM_005248251.2:c.659_660insACC	XP_005248308.1:p.Pro220_Pro221insPro
XM_005248252.1:c.617_618insACC	XP_005248309.1:p.Pro206_Pro207insPro
XM_005248253.1:c.386_387insACC	XP_005248310.1:p.Pro129_Pro130insPro
XM_011513967.1:c.386_387insACC	XP_011512269.1:p.Pro129_Pro130insPro
NM_001364128.1:c.167-20293_167-20292insACC	NP_001351057.1:n.167-20293_167-20292insACC
XM_005248251.3:c.659_660insACC	XP_005248308.1:p.Pro220_Pro221insPro
XM_005248252.2:c.617_618insACC	XP_005248309.1:p.Pro206_Pro207insPro
XM_011513967.2:c.386_387insACC	XP_011512269.1:p.Pro129_Pro130insPro
XM_017009072.1:c.440-20293_440-20292insACC	XP_016864561.1:n.440-20293_440-20292insACC
XM_017009073.1:c.398-20293_398-20292insACC	XP_016864562.1:n.398-20293_398-20292insACC
XM_017009074.1:c.440-20293_440-20292insACC	XP_016864563.1:n.440-20293_440-20292insACC
XM_017009075.2:c.167-20293_167-20292insACC	XP_016864564.1:n.167-20293_167-20292insACC
NM_001332.4:c.659_660insACC MANE Select	NP_001323.1:p.Pro220_Pro221insPro
NM_001288717.2:c.-123+11848_-123+11849insACC	NP_001275646.1:n.-123+11848_-123+11849insACC
NR_109988.2:n.1033-20293_1033-20292insACC
NM_001364128.2:c.167-20293_167-20292insACC	NP_001351057.1:n.167-20293_167-20292insACC