Canonical Allele Identifier: CA359278789

Gene: CTNND2

Linked Data

• MyVariant Identifiers: chr5:g.11346670G>T (hg19) ; chr5:g.11346558G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11346558G>T , CM000667.2:g.11346558G>T	GRCh38
NC_000005.9:g.11346670G>T , CM000667.1:g.11346670G>T	GRCh37
NC_000005.8:g.11399670G>T	NCBI36
NG_023544.1:g.562441C>A
NG_023544.2:g.562441C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.431C>A	ENSP00000516315.1:p.Ala144Asp
ENST00000706272.1:c.514C>A
ENST00000304623.13:c.1442C>A MANE Select	ENSP00000307134.8:p.Ala481Asp
ENST00000304623.12:c.1442C>A	ENSP00000307134.8:p.Ala481Asp
ENST00000495388.6:n.527C>A
ENST00000503622.5:c.431C>A	ENSP00000426887.1:p.Ala144Asp
ENST00000504354.5:n.481C>A
ENST00000504499.5:c.*181C>A	ENSP00000421000.1:n.*181C>A
ENST00000511377.5:c.1169C>A	ENSP00000426510.1:p.Ala390Asp
ENST00000513588.5:c.704C>A	ENSP00000421093.1:p.Ala235Asp
NM_001288715.1:c.1169C>A	NP_001275644.1:p.Ala390Asp
NM_001288716.1:c.431C>A	NP_001275645.1:p.Ala144Asp
NM_001288717.1:c.143C>A	NP_001275646.1:p.Ala48Asp
NM_001332.3:c.1442C>A	NP_001323.1:p.Ala481Asp
NR_109988.1:n.894C>A
XM_005248251.2:c.1442C>A	XP_005248308.1:p.Ala481Asp
XM_005248252.1:c.1400C>A	XP_005248309.1:p.Ala467Asp
XM_005248253.1:c.1169C>A	XP_005248310.1:p.Ala390Asp
XM_011513967.1:c.1169C>A	XP_011512269.1:p.Ala390Asp
NM_001364128.1:c.431C>A	NP_001351057.1:p.Ala144Asp
XM_005248251.3:c.1442C>A	XP_005248308.1:p.Ala481Asp
XM_005248252.2:c.1400C>A	XP_005248309.1:p.Ala467Asp
XM_011513967.2:c.1169C>A	XP_011512269.1:p.Ala390Asp
XM_017009072.1:c.704C>A	XP_016864561.1:p.Ala235Asp
XM_017009073.1:c.662C>A	XP_016864562.1:p.Ala221Asp
XM_017009074.1:c.704C>A	XP_016864563.1:p.Ala235Asp
XM_017009075.2:c.431C>A	XP_016864564.1:p.Ala144Asp
XM_024454368.1:c.-44+18138C>A	XP_024310136.1:n.-44+18138C>A
NM_001332.4:c.1442C>A MANE Select	NP_001323.1:p.Ala481Asp
NM_001288717.2:c.143C>A	NP_001275646.1:p.Ala48Asp
NR_109988.2:n.1297C>A
NM_001364128.2:c.431C>A	NP_001351057.1:p.Ala144Asp