Canonical Allele Identifier: CA347513713
Gene: CTNNA2 HGNC NCBI

Linked Data

gnomAD v4: 2-80581817-C-T
COSMIC: COSM197034 COSM3972372
MyVariant Identifiers: chr2:g.80808942C>T (hg19) chr2:g.80581817C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.80581817C>T , CM000664.2:g.80581817C>T GRCh38
NC_000002.11:g.80808942C>T , CM000664.1:g.80808942C>T GRCh37
NC_000002.10:g.80662453C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000402739.9:c.2005C>T MANE Select ENSP00000384638.4:p.Arg669Trp
ENST00000343114.7:c.1042C>T ENSP00000341500.3:p.Arg348Trp
ENST00000361291.8:c.853C>T ENSP00000355398.5:p.Arg285Trp
ENST00000402739.8:c.2005C>T ENSP00000384638.4:p.Arg669Trp
ENST00000466387.5:c.2005C>T ENSP00000418191.1:p.Arg669Trp
ENST00000496558.5:c.2005C>T ENSP00000419295.1:p.Arg669Trp
ENST00000540488.5:c.853C>T ENSP00000441705.2:p.Arg285Trp
ENST00000541047.5:c.901C>T ENSP00000444675.2:p.Arg301Trp
ENST00000629316.2:c.2005C>T ENSP00000486160.1:p.Arg669Trp
NM_001164883.1:c.2005C>T NP_001158355.1:p.Arg669Trp
NM_001282597.2:c.2005C>T NP_001269526.1:p.Arg669Trp
NM_001282598.1:c.2107C>T NP_001269527.1:p.Arg703Trp
NM_001282599.1:c.1042C>T NP_001269528.1:p.Arg348Trp
NM_001282600.1:c.901C>T NP_001269529.1:p.Arg301Trp
NM_004389.3:c.2005C>T NP_004380.2:p.Arg669Trp
XM_006711949.2:c.901C>T XP_006712012.1:p.Arg301Trp
XM_011532555.1:c.2005C>T XP_011530857.1:p.Arg669Trp
XM_011532556.1:c.2005C>T XP_011530858.1:p.Arg669Trp
XM_011532557.1:c.658C>T XP_011530859.1:p.Arg220Trp
NM_001320810.1:c.901C>T NP_001307739.1:p.Arg301Trp
XM_011532555.2:c.2005C>T XP_011530857.1:p.Arg669Trp
XM_011532556.2:c.2005C>T XP_011530858.1:p.Arg669Trp
XM_011532557.2:c.658C>T XP_011530859.1:p.Arg220Trp
XM_017003403.2:c.2005C>T XP_016858892.1:p.Arg669Trp
XM_017003404.2:c.2005C>T XP_016858893.1:p.Arg669Trp
XM_017003405.2:c.2005C>T XP_016858894.1:p.Arg669Trp
XM_017003406.2:c.901C>T XP_016858895.1:p.Arg301Trp
XM_024452714.1:c.2005C>T XP_024308482.1:p.Arg669Trp
XM_024452715.1:c.2005C>T XP_024308483.1:p.Arg669Trp
XM_024452716.1:c.2005C>T XP_024308484.1:p.Arg669Trp
NM_001164883.2:c.2005C>T NP_001158355.1:p.Arg669Trp
NM_001282597.3:c.2005C>T MANE Select NP_001269526.1:p.Arg669Trp
NM_001282598.2:c.2107C>T NP_001269527.1:p.Arg703Trp
NM_001282599.2:c.1042C>T NP_001269528.1:p.Arg348Trp
NM_001282600.2:c.901C>T NP_001269529.1:p.Arg301Trp
NM_001320810.2:c.901C>T NP_001307739.1:p.Arg301Trp
NM_004389.4:c.2005C>T NP_004380.2:p.Arg669Trp
NM_001399737.1:c.2005C>T NP_001386666.1:p.Arg669Trp
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