Canonical Allele Identifier: CA2982482785

Gene: CTNND2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11384798_11384800del , CM000667.2:g.11384798_11384800del	GRCh38
NC_000005.9:g.11384910_11384912del , CM000667.1:g.11384910_11384912del	GRCh37
NC_000005.8:g.11437910_11437912del	NCBI36
NG_023544.1:g.524200_524202del
NG_023544.2:g.524200_524202del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-19909_167-19907del	ENSP00000516315.1:n.167-19909_167-19907del
ENST00000706272.1:c.115_117del
ENST00000304623.13:c.1043_1045del MANE Select	ENSP00000307134.8:p.Gln348del
ENST00000304623.12:c.1043_1045del	ENSP00000307134.8:p.Gln348del
ENST00000502551.5:c.398-19909_398-19907del	ENSP00000422389.1:n.398-19909_398-19907del
ENST00000503622.5:c.167-19909_167-19907del	ENSP00000426887.1:n.167-19909_167-19907del
ENST00000504354.5:n.217-19909_217-19907del
ENST00000504499.5:c.612+12232_612+12234del	ENSP00000421000.1:n.612+12232_612+12234del
ENST00000506735.1:n.114_116del
ENST00000507430.1:n.139_141del
ENST00000511278.5:n.542-19909_542-19907del
ENST00000511377.5:c.770_772del	ENSP00000426510.1:p.Gln257del
ENST00000513588.5:c.440-19909_440-19907del	ENSP00000421093.1:n.440-19909_440-19907del
NM_001288715.1:c.770_772del	NP_001275644.1:p.Gln257del
NM_001288716.1:c.167-19909_167-19907del	NP_001275645.1:n.167-19909_167-19907del
NM_001288717.1:c.-123+12232_-123+12234del	NP_001275646.1:n.-123+12232_-123+12234del
NM_001332.3:c.1043_1045del	NP_001323.1:p.Gln348del
NR_109988.1:n.630-19909_630-19907del
XM_005248251.2:c.1043_1045del	XP_005248308.1:p.Gln348del
XM_005248252.1:c.1001_1003del	XP_005248309.1:p.Gln334del
XM_005248253.1:c.770_772del	XP_005248310.1:p.Gln257del
XM_011513967.1:c.770_772del	XP_011512269.1:p.Gln257del
NM_001364128.1:c.167-19909_167-19907del	NP_001351057.1:n.167-19909_167-19907del
XM_005248251.3:c.1043_1045del	XP_005248308.1:p.Gln348del
XM_005248252.2:c.1001_1003del	XP_005248309.1:p.Gln334del
XM_011513967.2:c.770_772del	XP_011512269.1:p.Gln257del
XM_017009072.1:c.440-19909_440-19907del	XP_016864561.1:n.440-19909_440-19907del
XM_017009073.1:c.398-19909_398-19907del	XP_016864562.1:n.398-19909_398-19907del
XM_017009074.1:c.440-19909_440-19907del	XP_016864563.1:n.440-19909_440-19907del
XM_017009075.2:c.167-19909_167-19907del	XP_016864564.1:n.167-19909_167-19907del
XM_024454368.1:c.-373_-371del	XP_024310136.1:n.-373_-371del
NM_001332.4:c.1043_1045del MANE Select	NP_001323.1:p.Gln348del
NM_001288717.2:c.-123+12232_-123+12234del	NP_001275646.1:n.-123+12232_-123+12234del
NR_109988.2:n.1033-19909_1033-19907del
NM_001364128.2:c.167-19909_167-19907del	NP_001351057.1:n.167-19909_167-19907del