Canonical Allele Identifier: CA359278680

Gene: CTNND2

Linked Data

• MyVariant Identifiers: chr5:g.11346615G>C (hg19) ; chr5:g.11346503G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11346503G>C , CM000667.2:g.11346503G>C	GRCh38
NC_000005.9:g.11346615G>C , CM000667.1:g.11346615G>C	GRCh37
NC_000005.8:g.11399615G>C	NCBI36
NG_023544.1:g.562496C>G
NG_023544.2:g.562496C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.486C>G	ENSP00000516315.1:p.Tyr162Ter
ENST00000706272.1:c.569C>G
ENST00000304623.13:c.1497C>G MANE Select	ENSP00000307134.8:p.Tyr499Ter
ENST00000304623.12:c.1497C>G	ENSP00000307134.8:p.Tyr499Ter
ENST00000495388.6:n.582C>G
ENST00000503622.5:c.486C>G	ENSP00000426887.1:p.Tyr162Ter
ENST00000504354.5:n.536C>G
ENST00000504499.5:c.*236C>G	ENSP00000421000.1:n.*236C>G
ENST00000511377.5:c.1224C>G	ENSP00000426510.1:p.Tyr408Ter
ENST00000513588.5:c.759C>G	ENSP00000421093.1:p.Tyr253Ter
NM_001288715.1:c.1224C>G	NP_001275644.1:p.Tyr408Ter
NM_001288716.1:c.486C>G	NP_001275645.1:p.Tyr162Ter
NM_001288717.1:c.198C>G	NP_001275646.1:p.Tyr66Ter
NM_001332.3:c.1497C>G	NP_001323.1:p.Tyr499Ter
NR_109988.1:n.949C>G
XM_005248251.2:c.1497C>G	XP_005248308.1:p.Tyr499Ter
XM_005248252.1:c.1455C>G	XP_005248309.1:p.Tyr485Ter
XM_005248253.1:c.1224C>G	XP_005248310.1:p.Tyr408Ter
XM_011513967.1:c.1224C>G	XP_011512269.1:p.Tyr408Ter
NM_001364128.1:c.486C>G	NP_001351057.1:p.Tyr162Ter
XM_005248251.3:c.1497C>G	XP_005248308.1:p.Tyr499Ter
XM_005248252.2:c.1455C>G	XP_005248309.1:p.Tyr485Ter
XM_011513967.2:c.1224C>G	XP_011512269.1:p.Tyr408Ter
XM_017009072.1:c.759C>G	XP_016864561.1:p.Tyr253Ter
XM_017009073.1:c.717C>G	XP_016864562.1:p.Tyr239Ter
XM_017009074.1:c.759C>G	XP_016864563.1:p.Tyr253Ter
XM_017009075.2:c.486C>G	XP_016864564.1:p.Tyr162Ter
XM_024454368.1:c.-44+18193C>G	XP_024310136.1:n.-44+18193C>G
NM_001332.4:c.1497C>G MANE Select	NP_001323.1:p.Tyr499Ter
NM_001288717.2:c.198C>G	NP_001275646.1:p.Tyr66Ter
NR_109988.2:n.1352C>G
NM_001364128.2:c.486C>G	NP_001351057.1:p.Tyr162Ter