Canonical Allele Identifier: CA2497098813

Gene: CTNND2

Linked Data

• dbSNP Id: rs1758919483

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11385064_11385072del , CM000667.2:g.11385064_11385072del	GRCh38
NC_000005.9:g.11385176_11385184del , CM000667.1:g.11385176_11385184del	GRCh37
NC_000005.8:g.11438176_11438184del	NCBI36
NG_023544.1:g.523929_523937del
NG_023544.2:g.523929_523937del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-20180_167-20172del	ENSP00000516315.1:n.167-20180_167-20172del
ENST00000304623.13:c.772_780del MANE Select	ENSP00000307134.8:p.Thr258_Pro260del
ENST00000304623.12:c.772_780del	ENSP00000307134.8:p.Thr258_Pro260del
ENST00000502551.5:c.398-20180_398-20172del	ENSP00000422389.1:n.398-20180_398-20172del
ENST00000503622.5:c.167-20180_167-20172del	ENSP00000426887.1:n.167-20180_167-20172del
ENST00000504354.5:n.217-20180_217-20172del
ENST00000504499.5:c.612+11961_612+11969del	ENSP00000421000.1:n.612+11961_612+11969del
ENST00000511278.5:n.542-20180_542-20172del
ENST00000511377.5:c.499_507del	ENSP00000426510.1:p.Thr167_Pro169del
ENST00000513588.5:c.440-20180_440-20172del	ENSP00000421093.1:n.440-20180_440-20172del
ENST00000513598.5:c.499_507del	ENSP00000426625.1:p.Thr167_Pro169del
ENST00000514132.1:n.421_429del
NM_001288715.1:c.499_507del	NP_001275644.1:p.Thr167_Pro169del
NM_001288716.1:c.167-20180_167-20172del	NP_001275645.1:n.167-20180_167-20172del
NM_001288717.1:c.-123+11961_-123+11969del	NP_001275646.1:n.-123+11961_-123+11969del
NM_001332.3:c.772_780del	NP_001323.1:p.Thr258_Pro260del
NR_109988.1:n.630-20180_630-20172del
XM_005248251.2:c.772_780del	XP_005248308.1:p.Thr258_Pro260del
XM_005248252.1:c.730_738del	XP_005248309.1:p.Thr244_Pro246del
XM_005248253.1:c.499_507del	XP_005248310.1:p.Thr167_Pro169del
XM_011513967.1:c.499_507del	XP_011512269.1:p.Thr167_Pro169del
NM_001364128.1:c.167-20180_167-20172del	NP_001351057.1:n.167-20180_167-20172del
XM_005248251.3:c.772_780del	XP_005248308.1:p.Thr258_Pro260del
XM_005248252.2:c.730_738del	XP_005248309.1:p.Thr244_Pro246del
XM_011513967.2:c.499_507del	XP_011512269.1:p.Thr167_Pro169del
XM_017009072.1:c.440-20180_440-20172del	XP_016864561.1:n.440-20180_440-20172del
XM_017009073.1:c.398-20180_398-20172del	XP_016864562.1:n.398-20180_398-20172del
XM_017009074.1:c.440-20180_440-20172del	XP_016864563.1:n.440-20180_440-20172del
XM_017009075.2:c.167-20180_167-20172del	XP_016864564.1:n.167-20180_167-20172del
NM_001332.4:c.772_780del MANE Select	NP_001323.1:p.Thr258_Pro260del
NM_001288717.2:c.-123+11961_-123+11969del	NP_001275646.1:n.-123+11961_-123+11969del
NR_109988.2:n.1033-20180_1033-20172del
NM_001364128.2:c.167-20180_167-20172del	NP_001351057.1:n.167-20180_167-20172del