Canonical Allele Identifier: CA5519759
Gene: CTNNA3 HGNC NCBI

Linked Data

ClinVar Variation Id: 240866
dbSNP Id: rs77165728

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.66103234C>T , CM000672.2:g.66103234C>T GRCh38
NC_000010.10:g.67862992C>T , CM000672.1:g.67862992C>T GRCh37
NC_000010.9:g.67532998C>T NCBI36
NG_034072.1:g.1597958G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682758.1:c.1900G>A ENSP00000508047.1:p.Glu634Lys
ENST00000682945.1:c.1699G>A ENSP00000506843.1:p.Glu567Lys
ENST00000683624.1:c.*1439G>A ENSP00000507406.1:n.*1439G>A
ENST00000683963.1:c.*1424G>A ENSP00000507029.1:n.*1424G>A
ENST00000684154.1:c.1900G>A ENSP00000508371.1:p.Glu634Lys
ENST00000433211.7:c.1900G>A MANE Select ENSP00000389714.1:p.Glu634Lys
ENST00000433211.6:c.1900G>A ENSP00000389714.1:p.Glu634Lys
NM_001127384.2:c.1900G>A NP_001120856.1:p.Glu634Lys
NM_013266.3:c.1900G>A NP_037398.2:p.Glu634Lys
XM_005269717.2:c.1936G>A XP_005269774.1:p.Glu646Lys
XM_011539721.1:c.2005G>A XP_011538023.1:p.Glu669Lys
XM_011539722.1:c.2005G>A XP_011538024.1:p.Glu669Lys
XM_011539723.1:c.1969G>A XP_011538025.1:p.Glu657Lys
XM_011539724.1:c.1969G>A XP_011538026.1:p.Glu657Lys
XM_011539725.1:c.1969G>A XP_011538027.1:p.Glu657Lys
XM_011539726.1:c.1936G>A XP_011538028.1:p.Glu646Lys
XM_011539727.1:c.1900G>A XP_011538029.1:p.Glu634Lys
XR_946024.1:n.415+4417C>T
XR_946025.1:n.415+4417C>T
XR_946026.1:n.415+4417C>T
XR_946027.1:n.415+4417C>T
XR_946028.1:n.415+4417C>T
XM_017016151.1:c.1969G>A XP_016871640.1:p.Glu657Lys
XM_017016152.1:c.2125G>A XP_016871641.1:p.Glu709Lys
XM_017016153.1:c.1936G>A XP_016871642.1:p.Glu646Lys
XM_017016154.1:c.1117G>A XP_016871643.1:p.Glu373Lys
XM_017016155.2:c.1117G>A XP_016871644.1:p.Glu373Lys
XM_017016156.1:c.1117G>A XP_016871645.1:p.Glu373Lys
XM_017016157.2:c.805G>A XP_016871646.1:p.Glu269Lys
XR_001747691.1:n.693+4417C>T
XR_001747692.2:n.693+4417C>T
XR_001747693.1:n.688+4417C>T
XR_001747694.1:n.693+4417C>T
XR_001747695.1:n.1411+4417C>T
XR_001747696.1:n.513+4417C>T
XR_001747697.1:n.1425+4417C>T
XR_001747698.1:n.518+4417C>T
XR_001747699.1:n.1403+4417C>T
XR_001747700.1:n.505+4417C>T
XR_001747702.1:n.693+4417C>T
XR_946026.2:n.693+4417C>T
XR_946027.2:n.693+4417C>T
NM_013266.4:c.1900G>A MANE Select NP_037398.2:p.Glu634Lys
NM_001127384.3:c.1900G>A NP_001120856.1:p.Glu634Lys