Canonical Allele Identifier: CA2497098814

Gene: CTNND2

Linked Data

• dbSNP Id: rs1758921240

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11385084_11385086del , CM000667.2:g.11385084_11385086del	GRCh38
NC_000005.9:g.11385196_11385198del , CM000667.1:g.11385196_11385198del	GRCh37
NC_000005.8:g.11438196_11438198del	NCBI36
NG_023544.1:g.523918_523920del
NG_023544.2:g.523918_523920del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-20191_167-20189del	ENSP00000516315.1:n.167-20191_167-20189del
ENST00000304623.13:c.761_763del MANE Select	ENSP00000307134.8:p.Tyr254del
ENST00000304623.12:c.761_763del	ENSP00000307134.8:p.Tyr254del
ENST00000502551.5:c.398-20191_398-20189del	ENSP00000422389.1:n.398-20191_398-20189del
ENST00000503622.5:c.167-20191_167-20189del	ENSP00000426887.1:n.167-20191_167-20189del
ENST00000504354.5:n.217-20191_217-20189del
ENST00000504499.5:c.612+11950_612+11952del	ENSP00000421000.1:n.612+11950_612+11952del
ENST00000511278.5:n.542-20191_542-20189del
ENST00000511377.5:c.488_490del	ENSP00000426510.1:p.Tyr163del
ENST00000513588.5:c.440-20191_440-20189del	ENSP00000421093.1:n.440-20191_440-20189del
ENST00000513598.5:c.488_490del	ENSP00000426625.1:p.Tyr163del
ENST00000514132.1:n.410_412del
NM_001288715.1:c.488_490del	NP_001275644.1:p.Tyr163del
NM_001288716.1:c.167-20191_167-20189del	NP_001275645.1:n.167-20191_167-20189del
NM_001288717.1:c.-123+11950_-123+11952del	NP_001275646.1:n.-123+11950_-123+11952del
NM_001332.3:c.761_763del	NP_001323.1:p.Tyr254del
NR_109988.1:n.630-20191_630-20189del
XM_005248251.2:c.761_763del	XP_005248308.1:p.Tyr254del
XM_005248252.1:c.719_721del	XP_005248309.1:p.Tyr240del
XM_005248253.1:c.488_490del	XP_005248310.1:p.Tyr163del
XM_011513967.1:c.488_490del	XP_011512269.1:p.Tyr163del
NM_001364128.1:c.167-20191_167-20189del	NP_001351057.1:n.167-20191_167-20189del
XM_005248251.3:c.761_763del	XP_005248308.1:p.Tyr254del
XM_005248252.2:c.719_721del	XP_005248309.1:p.Tyr240del
XM_011513967.2:c.488_490del	XP_011512269.1:p.Tyr163del
XM_017009072.1:c.440-20191_440-20189del	XP_016864561.1:n.440-20191_440-20189del
XM_017009073.1:c.398-20191_398-20189del	XP_016864562.1:n.398-20191_398-20189del
XM_017009074.1:c.440-20191_440-20189del	XP_016864563.1:n.440-20191_440-20189del
XM_017009075.2:c.167-20191_167-20189del	XP_016864564.1:n.167-20191_167-20189del
NM_001332.4:c.761_763del MANE Select	NP_001323.1:p.Tyr254del
NM_001288717.2:c.-123+11950_-123+11952del	NP_001275646.1:n.-123+11950_-123+11952del
NR_109988.2:n.1033-20191_1033-20189del
NM_001364128.2:c.167-20191_167-20189del	NP_001351057.1:n.167-20191_167-20189del