Canonical Allele Identifier: CA443541309

Gene: CTNND2

Linked Data

• dbSNP Id: rs1485865136
• MyVariant Identifiers: chr5:g.11346657G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11346545G>T , CM000667.2:g.11346545G>T	GRCh38
NC_000005.9:g.11346657G>T , CM000667.1:g.11346657G>T	GRCh37
NC_000005.8:g.11399657G>T	NCBI36
NG_023544.1:g.562454C>A
NG_023544.2:g.562454C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.444C>A	ENSP00000516315.1:p.Thr148=
ENST00000706272.1:c.527C>A
ENST00000304623.13:c.1455C>A MANE Select	ENSP00000307134.8:p.Thr485=
ENST00000304623.12:c.1455C>A	ENSP00000307134.8:p.Thr485=
ENST00000495388.6:n.540C>A
ENST00000503622.5:c.444C>A	ENSP00000426887.1:p.Thr148=
ENST00000504354.5:n.494C>A
ENST00000504499.5:c.*194C>A	ENSP00000421000.1:n.*194C>A
ENST00000511377.5:c.1182C>A	ENSP00000426510.1:p.Thr394=
ENST00000513588.5:c.717C>A	ENSP00000421093.1:p.Thr239=
NM_001288715.1:c.1182C>A	NP_001275644.1:p.Thr394=
NM_001288716.1:c.444C>A	NP_001275645.1:p.Thr148=
NM_001288717.1:c.156C>A	NP_001275646.1:p.Thr52=
NM_001332.3:c.1455C>A	NP_001323.1:p.Thr485=
NR_109988.1:n.907C>A
XM_005248251.2:c.1455C>A	XP_005248308.1:p.Thr485=
XM_005248252.1:c.1413C>A	XP_005248309.1:p.Thr471=
XM_005248253.1:c.1182C>A	XP_005248310.1:p.Thr394=
XM_011513967.1:c.1182C>A	XP_011512269.1:p.Thr394=
NM_001364128.1:c.444C>A	NP_001351057.1:p.Thr148=
XM_005248251.3:c.1455C>A	XP_005248308.1:p.Thr485=
XM_005248252.2:c.1413C>A	XP_005248309.1:p.Thr471=
XM_011513967.2:c.1182C>A	XP_011512269.1:p.Thr394=
XM_017009072.1:c.717C>A	XP_016864561.1:p.Thr239=
XM_017009073.1:c.675C>A	XP_016864562.1:p.Thr225=
XM_017009074.1:c.717C>A	XP_016864563.1:p.Thr239=
XM_017009075.2:c.444C>A	XP_016864564.1:p.Thr148=
XM_024454368.1:c.-44+18151C>A	XP_024310136.1:n.-44+18151C>A
NM_001332.4:c.1455C>A MANE Select	NP_001323.1:p.Thr485=
NM_001288717.2:c.156C>A	NP_001275646.1:p.Thr52=
NR_109988.2:n.1310C>A
NM_001364128.2:c.444C>A	NP_001351057.1:p.Thr148=