Canonical Allele Identifier: CA2765292194

Gene: CTNND2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11385070_11385114del , CM000667.2:g.11385070_11385114del	GRCh38
NC_000005.9:g.11385182_11385226del , CM000667.1:g.11385182_11385226del	GRCh37
NC_000005.8:g.11438182_11438226del	NCBI36
NG_023544.1:g.523888_523932del
NG_023544.2:g.523888_523932del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-20221_167-20177del	ENSP00000516315.1:n.167-20221_167-20177del
ENST00000304623.13:c.731_775del MANE Select	ENSP00000307134.8:p.Pro244_Thr258del
ENST00000304623.12:c.731_775del	ENSP00000307134.8:p.Pro244_Thr258del
ENST00000502551.5:c.398-20221_398-20177del	ENSP00000422389.1:n.398-20221_398-20177del
ENST00000503622.5:c.167-20221_167-20177del	ENSP00000426887.1:n.167-20221_167-20177del
ENST00000504354.5:n.217-20221_217-20177del
ENST00000504499.5:c.612+11920_612+11964del	ENSP00000421000.1:n.612+11920_612+11964del
ENST00000511278.5:n.542-20221_542-20177del
ENST00000511377.5:c.458_502del	ENSP00000426510.1:p.Pro153_Thr167del
ENST00000513588.5:c.440-20221_440-20177del	ENSP00000421093.1:n.440-20221_440-20177del
ENST00000513598.5:c.458_502del	ENSP00000426625.1:p.Pro153_Thr167del
ENST00000514132.1:n.380_424del
NM_001288715.1:c.458_502del	NP_001275644.1:p.Pro153_Thr167del
NM_001288716.1:c.167-20221_167-20177del	NP_001275645.1:n.167-20221_167-20177del
NM_001288717.1:c.-123+11920_-123+11964del	NP_001275646.1:n.-123+11920_-123+11964del
NM_001332.3:c.731_775del	NP_001323.1:p.Pro244_Thr258del
NR_109988.1:n.630-20221_630-20177del
XM_005248251.2:c.731_775del	XP_005248308.1:p.Pro244_Thr258del
XM_005248252.1:c.689_733del	XP_005248309.1:p.Pro230_Thr244del
XM_005248253.1:c.458_502del	XP_005248310.1:p.Pro153_Thr167del
XM_011513967.1:c.458_502del	XP_011512269.1:p.Pro153_Thr167del
NM_001364128.1:c.167-20221_167-20177del	NP_001351057.1:n.167-20221_167-20177del
XM_005248251.3:c.731_775del	XP_005248308.1:p.Pro244_Thr258del
XM_005248252.2:c.689_733del	XP_005248309.1:p.Pro230_Thr244del
XM_011513967.2:c.458_502del	XP_011512269.1:p.Pro153_Thr167del
XM_017009072.1:c.440-20221_440-20177del	XP_016864561.1:n.440-20221_440-20177del
XM_017009073.1:c.398-20221_398-20177del	XP_016864562.1:n.398-20221_398-20177del
XM_017009074.1:c.440-20221_440-20177del	XP_016864563.1:n.440-20221_440-20177del
XM_017009075.2:c.167-20221_167-20177del	XP_016864564.1:n.167-20221_167-20177del
NM_001332.4:c.731_775del MANE Select	NP_001323.1:p.Pro244_Thr258del
NM_001288717.2:c.-123+11920_-123+11964del	NP_001275646.1:n.-123+11920_-123+11964del
NR_109988.2:n.1033-20221_1033-20177del
NM_001364128.2:c.167-20221_167-20177del	NP_001351057.1:n.167-20221_167-20177del