Canonical Allele Identifier: CA359281355

Gene: CTNND2

Linked Data

• ClinVar Variation Id: 3078698
• ClinVar RCV Id: RCV004374987
• dbSNP Id: rs1758887287
• MyVariant Identifiers: chr5:g.11384980C>T (hg19) ; chr5:g.11384868C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11384868C>T , CM000667.2:g.11384868C>T	GRCh38
NC_000005.9:g.11384980C>T , CM000667.1:g.11384980C>T	GRCh37
NC_000005.8:g.11437980C>T	NCBI36
NG_023544.1:g.524131G>A
NG_023544.2:g.524131G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-19978G>A	ENSP00000516315.1:n.167-19978G>A
ENST00000706272.1:c.46G>A
ENST00000304623.13:c.974G>A MANE Select	ENSP00000307134.8:p.Gly325Asp
ENST00000304623.12:c.974G>A	ENSP00000307134.8:p.Gly325Asp
ENST00000502551.5:c.398-19978G>A	ENSP00000422389.1:n.398-19978G>A
ENST00000503622.5:c.167-19978G>A	ENSP00000426887.1:n.167-19978G>A
ENST00000504354.5:n.217-19978G>A
ENST00000504499.5:c.612+12163G>A	ENSP00000421000.1:n.612+12163G>A
ENST00000506735.1:n.45G>A
ENST00000507430.1:n.70G>A
ENST00000511278.5:n.542-19978G>A
ENST00000511377.5:c.701G>A	ENSP00000426510.1:p.Gly234Asp
ENST00000513588.5:c.440-19978G>A	ENSP00000421093.1:n.440-19978G>A
NM_001288715.1:c.701G>A	NP_001275644.1:p.Gly234Asp
NM_001288716.1:c.167-19978G>A	NP_001275645.1:n.167-19978G>A
NM_001288717.1:c.-123+12163G>A	NP_001275646.1:n.-123+12163G>A
NM_001332.3:c.974G>A	NP_001323.1:p.Gly325Asp
NR_109988.1:n.630-19978G>A
XM_005248251.2:c.974G>A	XP_005248308.1:p.Gly325Asp
XM_005248252.1:c.932G>A	XP_005248309.1:p.Gly311Asp
XM_005248253.1:c.701G>A	XP_005248310.1:p.Gly234Asp
XM_011513967.1:c.701G>A	XP_011512269.1:p.Gly234Asp
NM_001364128.1:c.167-19978G>A	NP_001351057.1:n.167-19978G>A
XM_005248251.3:c.974G>A	XP_005248308.1:p.Gly325Asp
XM_005248252.2:c.932G>A	XP_005248309.1:p.Gly311Asp
XM_011513967.2:c.701G>A	XP_011512269.1:p.Gly234Asp
XM_017009072.1:c.440-19978G>A	XP_016864561.1:n.440-19978G>A
XM_017009073.1:c.398-19978G>A	XP_016864562.1:n.398-19978G>A
XM_017009074.1:c.440-19978G>A	XP_016864563.1:n.440-19978G>A
XM_017009075.2:c.167-19978G>A	XP_016864564.1:n.167-19978G>A
XM_024454368.1:c.-442G>A	XP_024310136.1:n.-442G>A
NM_001332.4:c.974G>A MANE Select	NP_001323.1:p.Gly325Asp
NM_001288717.2:c.-123+12163G>A	NP_001275646.1:n.-123+12163G>A
NR_109988.2:n.1033-19978G>A
NM_001364128.2:c.167-19978G>A	NP_001351057.1:n.167-19978G>A