Canonical Allele Identifier: CA3201026
Gene: CTNND2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1260458
dbSNP Id: rs578098885

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.11385106_11385108dup , CM000667.2:g.11385106_11385108dup GRCh38
NC_000005.9:g.11385218_11385220dup , CM000667.1:g.11385218_11385220dup GRCh37
NC_000005.8:g.11438218_11438220dup NCBI36
NG_023544.1:g.523907_523909dup
NG_023544.2:g.523907_523909dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000706271.1:c.167-20202_167-20200dup ENSP00000516315.1:n.167-20202_167-20200dup
ENST00000304623.13:c.750_752dup MANE Select ENSP00000307134.8:p.Ala251_Leu252insAla
ENST00000304623.12:c.750_752dup ENSP00000307134.8:p.Ala251_Leu252insAla
ENST00000502551.5:c.398-20202_398-20200dup ENSP00000422389.1:n.398-20202_398-20200dup
ENST00000503622.5:c.167-20202_167-20200dup ENSP00000426887.1:n.167-20202_167-20200dup
ENST00000504354.5:n.217-20202_217-20200dup
ENST00000504499.5:c.612+11939_612+11941dup ENSP00000421000.1:n.612+11939_612+11941dup
ENST00000511278.5:n.542-20202_542-20200dup
ENST00000511377.5:c.477_479dup ENSP00000426510.1:p.Ala160_Leu161insAla
ENST00000513588.5:c.440-20202_440-20200dup ENSP00000421093.1:n.440-20202_440-20200dup
ENST00000513598.5:c.477_479dup ENSP00000426625.1:p.Ala160_Leu161insAla
ENST00000514132.1:n.399_401dup
NM_001288715.1:c.477_479dup NP_001275644.1:p.Ala160_Leu161insAla
NM_001288716.1:c.167-20202_167-20200dup NP_001275645.1:n.167-20202_167-20200dup
NM_001288717.1:c.-123+11939_-123+11941dup NP_001275646.1:n.-123+11939_-123+11941dup
NM_001332.3:c.750_752dup NP_001323.1:p.Ala251_Leu252insAla
NR_109988.1:n.630-20202_630-20200dup
XM_005248251.2:c.750_752dup XP_005248308.1:p.Ala251_Leu252insAla
XM_005248252.1:c.708_710dup XP_005248309.1:p.Ala237_Leu238insAla
XM_005248253.1:c.477_479dup XP_005248310.1:p.Ala160_Leu161insAla
XM_011513967.1:c.477_479dup XP_011512269.1:p.Ala160_Leu161insAla
NM_001364128.1:c.167-20202_167-20200dup NP_001351057.1:n.167-20202_167-20200dup
XM_005248251.3:c.750_752dup XP_005248308.1:p.Ala251_Leu252insAla
XM_005248252.2:c.708_710dup XP_005248309.1:p.Ala237_Leu238insAla
XM_011513967.2:c.477_479dup XP_011512269.1:p.Ala160_Leu161insAla
XM_017009072.1:c.440-20202_440-20200dup XP_016864561.1:n.440-20202_440-20200dup
XM_017009073.1:c.398-20202_398-20200dup XP_016864562.1:n.398-20202_398-20200dup
XM_017009074.1:c.440-20202_440-20200dup XP_016864563.1:n.440-20202_440-20200dup
XM_017009075.2:c.167-20202_167-20200dup XP_016864564.1:n.167-20202_167-20200dup
NM_001332.4:c.750_752dup MANE Select NP_001323.1:p.Ala251_Leu252insAla
NM_001288717.2:c.-123+11939_-123+11941dup NP_001275646.1:n.-123+11939_-123+11941dup
NR_109988.2:n.1033-20202_1033-20200dup
NM_001364128.2:c.167-20202_167-20200dup NP_001351057.1:n.167-20202_167-20200dup