Canonical Allele Identifier: CA1073213456

Gene: CTNND2

Linked Data

• gnomAD v3: 5-11385089-CGCGGCGGCGGCGGCGGCGGGCGGCGCGTCGGGCAGGTGGAAGGCGCTGCCCAGGCTGGGCGCGAACGGCTCCCGCG-C
• gnomAD v4: 5-11385089-CGCGGCGGCGGCGGCGGCGGGCGGCGCGTCGGGCAGGTGGAAGGCGCTGCCCAGGCTGGGCGCGAACGGCTCCCGCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11385109_11385184del , CM000667.2:g.11385109_11385184del	GRCh38
NC_000005.9:g.11385221_11385296del , CM000667.1:g.11385221_11385296del	GRCh37
NC_000005.8:g.11438221_11438296del	NCBI36
NG_023544.1:g.523834_523909del
NG_023544.2:g.523834_523909del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-20275_167-20200del	ENSP00000516315.1:n.167-20275_167-20200del
ENST00000304623.13:c.677_752del MANE Select	ENSP00000307134.8:p.Pro226ArgfsTer?
ENST00000304623.12:c.677_752del	ENSP00000307134.8:p.Pro226ArgfsTer?
ENST00000502551.5:c.398-20275_398-20200del	ENSP00000422389.1:n.398-20275_398-20200del
ENST00000503622.5:c.167-20275_167-20200del	ENSP00000426887.1:n.167-20275_167-20200del
ENST00000504354.5:n.217-20275_217-20200del
ENST00000504499.5:c.612+11866_612+11941del	ENSP00000421000.1:n.612+11866_612+11941del
ENST00000511278.5:n.542-20275_542-20200del
ENST00000511377.5:c.404_479del	ENSP00000426510.1:p.Pro135ArgfsTer?
ENST00000513588.5:c.440-20275_440-20200del	ENSP00000421093.1:n.440-20275_440-20200del
ENST00000513598.5:c.404_479del	ENSP00000426625.1:p.Pro135ArgfsTer?
ENST00000514132.1:n.326_401del
NM_001288715.1:c.404_479del	NP_001275644.1:p.Pro135ArgfsTer?
NM_001288716.1:c.167-20275_167-20200del	NP_001275645.1:n.167-20275_167-20200del
NM_001288717.1:c.-123+11866_-123+11941del	NP_001275646.1:n.-123+11866_-123+11941del
NM_001332.3:c.677_752del	NP_001323.1:p.Pro226ArgfsTer?
NR_109988.1:n.630-20275_630-20200del
XM_005248251.2:c.677_752del	XP_005248308.1:p.Pro226ArgfsTer?
XM_005248252.1:c.635_710del	XP_005248309.1:p.Pro212ArgfsTer?
XM_005248253.1:c.404_479del	XP_005248310.1:p.Pro135ArgfsTer?
XM_011513967.1:c.404_479del	XP_011512269.1:p.Pro135ArgfsTer?
NM_001364128.1:c.167-20275_167-20200del	NP_001351057.1:n.167-20275_167-20200del
XM_005248251.3:c.677_752del	XP_005248308.1:p.Pro226ArgfsTer?
XM_005248252.2:c.635_710del	XP_005248309.1:p.Pro212ArgfsTer?
XM_011513967.2:c.404_479del	XP_011512269.1:p.Pro135ArgfsTer?
XM_017009072.1:c.440-20275_440-20200del	XP_016864561.1:n.440-20275_440-20200del
XM_017009073.1:c.398-20275_398-20200del	XP_016864562.1:n.398-20275_398-20200del
XM_017009074.1:c.440-20275_440-20200del	XP_016864563.1:n.440-20275_440-20200del
XM_017009075.2:c.167-20275_167-20200del	XP_016864564.1:n.167-20275_167-20200del
NM_001332.4:c.677_752del MANE Select	NP_001323.1:p.Pro226ArgfsTer?
NM_001288717.2:c.-123+11866_-123+11941del	NP_001275646.1:n.-123+11866_-123+11941del
NR_109988.2:n.1033-20275_1033-20200del
NM_001364128.2:c.167-20275_167-20200del	NP_001351057.1:n.167-20275_167-20200del