Canonical Allele Identifier: CA16219025
Gene: CTNND2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1012176

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.11320426G>T , CM000667.2:g.11320426G>T GRCh38
NC_000005.9:g.11320538G>T , CM000667.1:g.11320538G>T GRCh37
NC_000005.8:g.11373538G>T NCBI36
NG_023544.1:g.588573C>A

Transcript Alleles

HGVS Amino-acid change
NM_001288715.1:c.1355+25946C>A VV NP_001275644.1:p.=
NM_001288716.1:c.617+25946C>A VV NP_001275645.1:p.=
NM_001288717.1:c.329+25946C>A VV NP_001275646.1:p.=
NM_001332.3:c.1628+25946C>A VV NP_001323.1:p.=
NR_109988.1:n.1080+25946C>A
XM_005248251.2:c.1628+25946C>A XP_005248308.1:p.=
XM_005248252.1:c.1586+25946C>A XP_005248309.1:p.=
XM_005248253.1:c.1355+25946C>A XP_005248310.1:p.=
XM_011513967.1:c.1355+25946C>A XP_011512269.1:p.=
NM_001364128.1:c.617+25946C>A VV NP_001351057.1:p.=
XM_005248251.3:c.1628+25946C>A
XM_005248252.2:c.1586+25946C>A
XM_011513967.2:c.1355+25946C>A
XM_017009072.1:c.890+25946C>A XP_016864561.1:p.=
XM_017009073.1:c.848+25946C>A XP_016864562.1:p.=
XM_017009074.1:c.890+25946C>A XP_016864563.1:p.=
XM_017009075.2:c.617+25946C>A XP_016864564.1:p.=
XM_024454368.1:c.-44+44270C>A XP_024310136.1:p.=
ENST00000304623.12:c.1628+25946C>A ENSP00000307134.8:p.=
ENST00000495388.6:n.713+25946C>A
ENST00000503622.5:c.617+25946C>A ENSP00000426887.1:p.=
ENST00000504499.5:c.*367+25946C>A ENSP00000421000.1:p.=
ENST00000511377.5:c.1355+25946C>A ENSP00000426510.1:p.=
ENST00000513588.5:c.890+25946C>A ENSP00000421093.1:p.=