Canonical Allele Identifier: CA359281518
Gene: CTNND2 HGNC NCBI

Linked Data

gnomAD v4: 5-11384944-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.11384944G>T , CM000667.2:g.11384944G>T GRCh38
NC_000005.9:g.11385056G>T , CM000667.1:g.11385056G>T GRCh37
NC_000005.8:g.11438056G>T NCBI36
NG_023544.1:g.524055C>A
NG_023544.2:g.524055C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706271.1:c.167-20054C>A ENSP00000516315.1:n.167-20054C>A
ENST00000304623.13:c.898C>A MANE Select ENSP00000307134.8:p.Pro300Thr
ENST00000304623.12:c.898C>A ENSP00000307134.8:p.Pro300Thr
ENST00000502551.5:c.398-20054C>A ENSP00000422389.1:n.398-20054C>A
ENST00000503622.5:c.167-20054C>A ENSP00000426887.1:n.167-20054C>A
ENST00000504354.5:n.217-20054C>A
ENST00000504499.5:c.612+12087C>A ENSP00000421000.1:n.612+12087C>A
ENST00000511278.5:n.542-20054C>A
ENST00000511377.5:c.625C>A ENSP00000426510.1:p.Pro209Thr
ENST00000513588.5:c.440-20054C>A ENSP00000421093.1:n.440-20054C>A
NM_001288715.1:c.625C>A NP_001275644.1:p.Pro209Thr
NM_001288716.1:c.167-20054C>A NP_001275645.1:n.167-20054C>A
NM_001288717.1:c.-123+12087C>A NP_001275646.1:n.-123+12087C>A
NM_001332.3:c.898C>A NP_001323.1:p.Pro300Thr
NR_109988.1:n.630-20054C>A
XM_005248251.2:c.898C>A XP_005248308.1:p.Pro300Thr
XM_005248252.1:c.856C>A XP_005248309.1:p.Pro286Thr
XM_005248253.1:c.625C>A XP_005248310.1:p.Pro209Thr
XM_011513967.1:c.625C>A XP_011512269.1:p.Pro209Thr
NM_001364128.1:c.167-20054C>A NP_001351057.1:n.167-20054C>A
XM_005248251.3:c.898C>A XP_005248308.1:p.Pro300Thr
XM_005248252.2:c.856C>A XP_005248309.1:p.Pro286Thr
XM_011513967.2:c.625C>A XP_011512269.1:p.Pro209Thr
XM_017009072.1:c.440-20054C>A XP_016864561.1:n.440-20054C>A
XM_017009073.1:c.398-20054C>A XP_016864562.1:n.398-20054C>A
XM_017009074.1:c.440-20054C>A XP_016864563.1:n.440-20054C>A
XM_017009075.2:c.167-20054C>A XP_016864564.1:n.167-20054C>A
NM_001332.4:c.898C>A MANE Select NP_001323.1:p.Pro300Thr
NM_001288717.2:c.-123+12087C>A NP_001275646.1:n.-123+12087C>A
NR_109988.2:n.1033-20054C>A
NM_001364128.2:c.167-20054C>A NP_001351057.1:n.167-20054C>A