Canonical Allele Identifier: CA2673260098

Gene: CTNND2

Linked Data

• gnomAD v4: 5-11385179-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11385181del , CM000667.2:g.11385181del	GRCh38
NC_000005.9:g.11385293del , CM000667.1:g.11385293del	GRCh37
NC_000005.8:g.11438293del	NCBI36
NG_023544.1:g.523819del
NG_023544.2:g.523819del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-20290del	ENSP00000516315.1:n.167-20290del
ENST00000304623.13:c.662del MANE Select	ENSP00000307134.8:p.Pro221ArgfsTer?
ENST00000304623.12:c.662del	ENSP00000307134.8:p.Pro221ArgfsTer?
ENST00000502551.5:c.398-20290del	ENSP00000422389.1:n.398-20290del
ENST00000503622.5:c.167-20290del	ENSP00000426887.1:n.167-20290del
ENST00000504354.5:n.217-20290del
ENST00000504499.5:c.612+11851del	ENSP00000421000.1:n.612+11851del
ENST00000511278.5:n.542-20290del
ENST00000511377.5:c.389del	ENSP00000426510.1:p.Pro130ArgfsTer?
ENST00000513588.5:c.440-20290del	ENSP00000421093.1:n.440-20290del
ENST00000513598.5:c.389del	ENSP00000426625.1:p.Pro130ArgfsTer?
ENST00000514132.1:n.311del
NM_001288715.1:c.389del	NP_001275644.1:p.Pro130ArgfsTer?
NM_001288716.1:c.167-20290del	NP_001275645.1:n.167-20290del
NM_001288717.1:c.-123+11851del	NP_001275646.1:n.-123+11851del
NM_001332.3:c.662del	NP_001323.1:p.Pro221ArgfsTer?
NR_109988.1:n.630-20290del
XM_005248251.2:c.662del	XP_005248308.1:p.Pro221ArgfsTer?
XM_005248252.1:c.620del	XP_005248309.1:p.Pro207ArgfsTer?
XM_005248253.1:c.389del	XP_005248310.1:p.Pro130ArgfsTer?
XM_011513967.1:c.389del	XP_011512269.1:p.Pro130ArgfsTer?
NM_001364128.1:c.167-20290del	NP_001351057.1:n.167-20290del
XM_005248251.3:c.662del	XP_005248308.1:p.Pro221ArgfsTer?
XM_005248252.2:c.620del	XP_005248309.1:p.Pro207ArgfsTer?
XM_011513967.2:c.389del	XP_011512269.1:p.Pro130ArgfsTer?
XM_017009072.1:c.440-20290del	XP_016864561.1:n.440-20290del
XM_017009073.1:c.398-20290del	XP_016864562.1:n.398-20290del
XM_017009074.1:c.440-20290del	XP_016864563.1:n.440-20290del
XM_017009075.2:c.167-20290del	XP_016864564.1:n.167-20290del
NM_001332.4:c.662del MANE Select	NP_001323.1:p.Pro221ArgfsTer?
NM_001288717.2:c.-123+11851del	NP_001275646.1:n.-123+11851del
NR_109988.2:n.1033-20290del
NM_001364128.2:c.167-20290del	NP_001351057.1:n.167-20290del