Canonical Allele Identifier: CA359278740

Gene: CTNND2

Linked Data

• MyVariant Identifiers: chr5:g.11346644T>G (hg19) ; chr5:g.11346532T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11346532T>G , CM000667.2:g.11346532T>G	GRCh38
NC_000005.9:g.11346644T>G , CM000667.1:g.11346644T>G	GRCh37
NC_000005.8:g.11399644T>G	NCBI36
NG_023544.1:g.562467A>C
NG_023544.2:g.562467A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.457A>C	ENSP00000516315.1:p.Ser153Arg
ENST00000706272.1:c.540A>C
ENST00000304623.13:c.1468A>C MANE Select	ENSP00000307134.8:p.Ser490Arg
ENST00000304623.12:c.1468A>C	ENSP00000307134.8:p.Ser490Arg
ENST00000495388.6:n.553A>C
ENST00000503622.5:c.457A>C	ENSP00000426887.1:p.Ser153Arg
ENST00000504354.5:n.507A>C
ENST00000504499.5:c.*207A>C	ENSP00000421000.1:n.*207A>C
ENST00000511377.5:c.1195A>C	ENSP00000426510.1:p.Ser399Arg
ENST00000513588.5:c.730A>C	ENSP00000421093.1:p.Ser244Arg
NM_001288715.1:c.1195A>C	NP_001275644.1:p.Ser399Arg
NM_001288716.1:c.457A>C	NP_001275645.1:p.Ser153Arg
NM_001288717.1:c.169A>C	NP_001275646.1:p.Ser57Arg
NM_001332.3:c.1468A>C	NP_001323.1:p.Ser490Arg
NR_109988.1:n.920A>C
XM_005248251.2:c.1468A>C	XP_005248308.1:p.Ser490Arg
XM_005248252.1:c.1426A>C	XP_005248309.1:p.Ser476Arg
XM_005248253.1:c.1195A>C	XP_005248310.1:p.Ser399Arg
XM_011513967.1:c.1195A>C	XP_011512269.1:p.Ser399Arg
NM_001364128.1:c.457A>C	NP_001351057.1:p.Ser153Arg
XM_005248251.3:c.1468A>C	XP_005248308.1:p.Ser490Arg
XM_005248252.2:c.1426A>C	XP_005248309.1:p.Ser476Arg
XM_011513967.2:c.1195A>C	XP_011512269.1:p.Ser399Arg
XM_017009072.1:c.730A>C	XP_016864561.1:p.Ser244Arg
XM_017009073.1:c.688A>C	XP_016864562.1:p.Ser230Arg
XM_017009074.1:c.730A>C	XP_016864563.1:p.Ser244Arg
XM_017009075.2:c.457A>C	XP_016864564.1:p.Ser153Arg
XM_024454368.1:c.-44+18164A>C	XP_024310136.1:n.-44+18164A>C
NM_001332.4:c.1468A>C MANE Select	NP_001323.1:p.Ser490Arg
NM_001288717.2:c.169A>C	NP_001275646.1:p.Ser57Arg
NR_109988.2:n.1323A>C
NM_001364128.2:c.457A>C	NP_001351057.1:p.Ser153Arg