Canonical Allele Identifier: CA359281516
Gene: CTNND2 HGNC NCBI

Linked Data

dbSNP Id: rs1412494769
gnomAD v2: 5-11385056-G-A
gnomAD v4: 5-11384944-G-A

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000706271.1:c.167-20054C>T ENSP00000516315.1:n.167-20054C>T
ENST00000304623.13:c.898C>T MANE Select ENSP00000307134.8:p.Pro300Ser
ENST00000304623.12:c.898C>T ENSP00000307134.8:p.Pro300Ser
ENST00000502551.5:c.398-20054C>T ENSP00000422389.1:n.398-20054C>T
ENST00000503622.5:c.167-20054C>T ENSP00000426887.1:n.167-20054C>T
ENST00000504354.5:n.217-20054C>T
ENST00000504499.5:c.612+12087C>T ENSP00000421000.1:n.612+12087C>T
ENST00000511278.5:n.542-20054C>T
ENST00000511377.5:c.625C>T ENSP00000426510.1:p.Pro209Ser
ENST00000513588.5:c.440-20054C>T ENSP00000421093.1:n.440-20054C>T
NM_001288715.1:c.625C>T NP_001275644.1:p.Pro209Ser
NM_001288716.1:c.167-20054C>T NP_001275645.1:n.167-20054C>T
NM_001288717.1:c.-123+12087C>T NP_001275646.1:n.-123+12087C>T
NM_001332.3:c.898C>T NP_001323.1:p.Pro300Ser
NR_109988.1:n.630-20054C>T
XM_005248251.2:c.898C>T XP_005248308.1:p.Pro300Ser
XM_005248252.1:c.856C>T XP_005248309.1:p.Pro286Ser
XM_005248253.1:c.625C>T XP_005248310.1:p.Pro209Ser
XM_011513967.1:c.625C>T XP_011512269.1:p.Pro209Ser
NM_001364128.1:c.167-20054C>T NP_001351057.1:n.167-20054C>T
XM_005248251.3:c.898C>T XP_005248308.1:p.Pro300Ser
XM_005248252.2:c.856C>T XP_005248309.1:p.Pro286Ser
XM_011513967.2:c.625C>T XP_011512269.1:p.Pro209Ser
XM_017009072.1:c.440-20054C>T XP_016864561.1:n.440-20054C>T
XM_017009073.1:c.398-20054C>T XP_016864562.1:n.398-20054C>T
XM_017009074.1:c.440-20054C>T XP_016864563.1:n.440-20054C>T
XM_017009075.2:c.167-20054C>T XP_016864564.1:n.167-20054C>T
NM_001332.4:c.898C>T MANE Select NP_001323.1:p.Pro300Ser
NM_001288717.2:c.-123+12087C>T NP_001275646.1:n.-123+12087C>T
NR_109988.2:n.1033-20054C>T
NM_001364128.2:c.167-20054C>T NP_001351057.1:n.167-20054C>T