Canonical Allele Identifier: CA2497098810

Gene: CTNND2

Linked Data

• dbSNP Id: rs1758875264

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11384802_11384804dup , CM000667.2:g.11384802_11384804dup	GRCh38
NC_000005.9:g.11384914_11384916dup , CM000667.1:g.11384914_11384916dup	GRCh37
NC_000005.8:g.11437914_11437916dup	NCBI36
NG_023544.1:g.524198_524200dup
NG_023544.2:g.524198_524200dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-19911_167-19909dup	ENSP00000516315.1:n.167-19911_167-19909dup
ENST00000706272.1:c.113_115dup
ENST00000304623.13:c.1041_1043dup MANE Select	ENSP00000307134.8:p.His347_Gln348insHis
ENST00000304623.12:c.1041_1043dup	ENSP00000307134.8:p.His347_Gln348insHis
ENST00000502551.5:c.398-19911_398-19909dup	ENSP00000422389.1:n.398-19911_398-19909dup
ENST00000503622.5:c.167-19911_167-19909dup	ENSP00000426887.1:n.167-19911_167-19909dup
ENST00000504354.5:n.217-19911_217-19909dup
ENST00000504499.5:c.612+12230_612+12232dup	ENSP00000421000.1:n.612+12230_612+12232dup
ENST00000506735.1:n.112_114dup
ENST00000507430.1:n.137_139dup
ENST00000511278.5:n.542-19911_542-19909dup
ENST00000511377.5:c.768_770dup	ENSP00000426510.1:p.His256_Gln257insHis
ENST00000513588.5:c.440-19911_440-19909dup	ENSP00000421093.1:n.440-19911_440-19909dup
NM_001288715.1:c.768_770dup	NP_001275644.1:p.His256_Gln257insHis
NM_001288716.1:c.167-19911_167-19909dup	NP_001275645.1:n.167-19911_167-19909dup
NM_001288717.1:c.-123+12230_-123+12232dup	NP_001275646.1:n.-123+12230_-123+12232dup
NM_001332.3:c.1041_1043dup	NP_001323.1:p.His347_Gln348insHis
NR_109988.1:n.630-19911_630-19909dup
XM_005248251.2:c.1041_1043dup	XP_005248308.1:p.His347_Gln348insHis
XM_005248252.1:c.999_1001dup	XP_005248309.1:p.His333_Gln334insHis
XM_005248253.1:c.768_770dup	XP_005248310.1:p.His256_Gln257insHis
XM_011513967.1:c.768_770dup	XP_011512269.1:p.His256_Gln257insHis
NM_001364128.1:c.167-19911_167-19909dup	NP_001351057.1:n.167-19911_167-19909dup
XM_005248251.3:c.1041_1043dup	XP_005248308.1:p.His347_Gln348insHis
XM_005248252.2:c.999_1001dup	XP_005248309.1:p.His333_Gln334insHis
XM_011513967.2:c.768_770dup	XP_011512269.1:p.His256_Gln257insHis
XM_017009072.1:c.440-19911_440-19909dup	XP_016864561.1:n.440-19911_440-19909dup
XM_017009073.1:c.398-19911_398-19909dup	XP_016864562.1:n.398-19911_398-19909dup
XM_017009074.1:c.440-19911_440-19909dup	XP_016864563.1:n.440-19911_440-19909dup
XM_017009075.2:c.167-19911_167-19909dup	XP_016864564.1:n.167-19911_167-19909dup
XM_024454368.1:c.-375_-373dup	XP_024310136.1:n.-375_-373dup
NM_001332.4:c.1041_1043dup MANE Select	NP_001323.1:p.His347_Gln348insHis
NM_001288717.2:c.-123+12230_-123+12232dup	NP_001275646.1:n.-123+12230_-123+12232dup
NR_109988.2:n.1033-19911_1033-19909dup
NM_001364128.2:c.167-19911_167-19909dup	NP_001351057.1:n.167-19911_167-19909dup