Canonical Allele Identifier: CA2673260070

Gene: CTNND2

Linked Data

• gnomAD v4: 5-11385097-CGGCGGCGGCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11385105_11385114del , CM000667.2:g.11385105_11385114del	GRCh38
NC_000005.9:g.11385217_11385226del , CM000667.1:g.11385217_11385226del	GRCh37
NC_000005.8:g.11438217_11438226del	NCBI36
NG_023544.1:g.523892_523901del
NG_023544.2:g.523892_523901del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-20217_167-20208del	ENSP00000516315.1:n.167-20217_167-20208del
ENST00000304623.13:c.735_744del MANE Select	ENSP00000307134.8:p.Ala246ProfsTer?
ENST00000304623.12:c.735_744del	ENSP00000307134.8:p.Ala246ProfsTer?
ENST00000502551.5:c.398-20217_398-20208del	ENSP00000422389.1:n.398-20217_398-20208del
ENST00000503622.5:c.167-20217_167-20208del	ENSP00000426887.1:n.167-20217_167-20208del
ENST00000504354.5:n.217-20217_217-20208del
ENST00000504499.5:c.612+11924_612+11933del	ENSP00000421000.1:n.612+11924_612+11933del
ENST00000511278.5:n.542-20217_542-20208del
ENST00000511377.5:c.462_471del	ENSP00000426510.1:p.Ala155ProfsTer?
ENST00000513588.5:c.440-20217_440-20208del	ENSP00000421093.1:n.440-20217_440-20208del
ENST00000513598.5:c.462_471del	ENSP00000426625.1:p.Ala155ProfsTer?
ENST00000514132.1:n.384_393del
NM_001288715.1:c.462_471del	NP_001275644.1:p.Ala155ProfsTer?
NM_001288716.1:c.167-20217_167-20208del	NP_001275645.1:n.167-20217_167-20208del
NM_001288717.1:c.-123+11924_-123+11933del	NP_001275646.1:n.-123+11924_-123+11933del
NM_001332.3:c.735_744del	NP_001323.1:p.Ala246ProfsTer?
NR_109988.1:n.630-20217_630-20208del
XM_005248251.2:c.735_744del	XP_005248308.1:p.Ala246ProfsTer?
XM_005248252.1:c.693_702del	XP_005248309.1:p.Ala232ProfsTer?
XM_005248253.1:c.462_471del	XP_005248310.1:p.Ala155ProfsTer?
XM_011513967.1:c.462_471del	XP_011512269.1:p.Ala155ProfsTer?
NM_001364128.1:c.167-20217_167-20208del	NP_001351057.1:n.167-20217_167-20208del
XM_005248251.3:c.735_744del	XP_005248308.1:p.Ala246ProfsTer?
XM_005248252.2:c.693_702del	XP_005248309.1:p.Ala232ProfsTer?
XM_011513967.2:c.462_471del	XP_011512269.1:p.Ala155ProfsTer?
XM_017009072.1:c.440-20217_440-20208del	XP_016864561.1:n.440-20217_440-20208del
XM_017009073.1:c.398-20217_398-20208del	XP_016864562.1:n.398-20217_398-20208del
XM_017009074.1:c.440-20217_440-20208del	XP_016864563.1:n.440-20217_440-20208del
XM_017009075.2:c.167-20217_167-20208del	XP_016864564.1:n.167-20217_167-20208del
NM_001332.4:c.735_744del MANE Select	NP_001323.1:p.Ala246ProfsTer?
NM_001288717.2:c.-123+11924_-123+11933del	NP_001275646.1:n.-123+11924_-123+11933del
NR_109988.2:n.1033-20217_1033-20208del
NM_001364128.2:c.167-20217_167-20208del	NP_001351057.1:n.167-20217_167-20208del