Canonical Allele Identifier: CA11920922
Gene: CTNND2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.11169833C>T , CM000667.2:g.11169833C>T GRCh38
NC_000005.9:g.11169945C>T , CM000667.1:g.11169945C>T GRCh37
NC_000005.8:g.11222945C>T NCBI36
NG_023544.1:g.739166G>A
NG_023544.2:g.739166G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706271.1:c.965-10074G>A ENSP00000516315.1:n.965-10074G>A
ENST00000706272.1:c.1048-10074G>A
ENST00000304623.13:c.1976-10074G>A MANE Select ENSP00000307134.8:n.1976-10074G>A
ENST00000304623.12:c.1976-10074G>A ENSP00000307134.8:n.1976-10074G>A
ENST00000495388.6:n.1061-10074G>A
ENST00000503622.5:c.965-10074G>A ENSP00000426887.1:n.965-10074G>A
ENST00000504499.5:c.*715-10074G>A ENSP00000421000.1:n.*715-10074G>A
ENST00000511377.5:c.1703-10074G>A ENSP00000426510.1:n.1703-10074G>A
ENST00000513588.5:c.1238-10074G>A ENSP00000421093.1:n.1238-10074G>A
NM_001288715.1:c.1703-10074G>A NP_001275644.1:n.1703-10074G>A
NM_001288716.1:c.965-10074G>A NP_001275645.1:n.965-10074G>A
NM_001288717.1:c.677-10074G>A NP_001275646.1:n.677-10074G>A
NM_001332.3:c.1976-10074G>A NP_001323.1:n.1976-10074G>A
NR_109988.1:n.1428-10074G>A
XM_005248251.2:c.1976-10074G>A XP_005248308.1:n.1976-10074G>A
XM_005248252.1:c.1934-10074G>A XP_005248309.1:n.1934-10074G>A
XM_005248253.1:c.1703-10074G>A XP_005248310.1:n.1703-10074G>A
XM_011513967.1:c.1703-10074G>A XP_011512269.1:n.1703-10074G>A
NM_001364128.1:c.965-10074G>A NP_001351057.1:n.965-10074G>A
XM_005248251.3:c.1976-10074G>A XP_005248308.1:n.1976-10074G>A
XM_005248252.2:c.1934-10074G>A XP_005248309.1:n.1934-10074G>A
XM_011513967.2:c.1703-10074G>A XP_011512269.1:n.1703-10074G>A
XM_017009072.1:c.1238-10074G>A XP_016864561.1:n.1238-10074G>A
XM_017009073.1:c.1196-10074G>A XP_016864562.1:n.1196-10074G>A
XM_017009074.1:c.1238-10074G>A XP_016864563.1:n.1238-10074G>A
XM_017009075.2:c.965-10074G>A XP_016864564.1:n.965-10074G>A
XM_024454368.1:c.305-10074G>A XP_024310136.1:n.305-10074G>A
NM_001332.4:c.1976-10074G>A MANE Select NP_001323.1:n.1976-10074G>A
NM_001288717.2:c.677-10074G>A NP_001275646.1:n.677-10074G>A
NR_109988.2:n.1831-10074G>A
NM_001364128.2:c.965-10074G>A NP_001351057.1:n.965-10074G>A
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