Canonical Allele Identifier: CA51169792
Gene: CTNNA2 HGNC NCBI

Linked Data

dbSNP Id: rs1446109

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.80311294A>G , CM000664.2:g.80311294A>G GRCh38
NC_000002.11:g.80538419A>G , CM000664.1:g.80538419A>G GRCh37
NC_000002.10:g.80391930A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000402739.9:c.1057-81917A>G MANE Select ENSP00000384638.4:p.=
ENST00000402739.8:c.1057-81917A>G ENSP00000384638.4:p.=
ENST00000466387.5:c.1057-81917A>G ENSP00000418191.1:p.=
ENST00000493024.5:n.206+5971A>G
ENST00000496558.5:c.1057-81917A>G ENSP00000419295.1:p.=
ENST00000541047.5:c.-49+5971A>G ENSP00000444675.2:p.=
ENST00000629316.2:c.1057-81917A>G ENSP00000486160.1:p.=
NM_001164883.1:c.1057-81917A>G NP_001158355.1:p.=
NM_001282597.2:c.1057-81917A>G NP_001269526.1:p.=
NM_001282598.1:c.1159-81917A>G NP_001269527.1:p.=
NM_001282600.1:c.-49+5971A>G NP_001269529.1:p.=
NM_004389.3:c.1057-81917A>G NP_004380.2:p.=
XM_006711949.2:c.-49+5971A>G XP_006712012.1:p.=
XM_011532555.1:c.1057-81917A>G XP_011530857.1:p.=
XM_011532556.1:c.1057-81917A>G XP_011530858.1:p.=
NM_001320810.1:c.-49+5971A>G NP_001307739.1:p.=
XM_011532555.2:c.1057-81917A>G XP_011530857.1:p.=
XM_011532556.2:c.1057-81917A>G XP_011530858.1:p.=
XM_017003403.2:c.1057-81917A>G XP_016858892.1:p.=
XM_017003404.2:c.1057-81917A>G XP_016858893.1:p.=
XM_017003405.2:c.1057-81917A>G XP_016858894.1:p.=
XM_017003406.2:c.-49+5971A>G XP_016858895.1:p.=
XM_024452714.1:c.1057-81917A>G XP_024308482.1:p.=
XM_024452715.1:c.1057-81917A>G XP_024308483.1:p.=
XM_024452716.1:c.1057-81917A>G XP_024308484.1:p.=
NM_001164883.2:c.1057-81917A>G NP_001158355.1:p.=
NM_001282597.3:c.1057-81917A>G MANE Select NP_001269526.1:p.=
NM_001282598.2:c.1159-81917A>G NP_001269527.1:p.=
NM_001282600.2:c.-49+5971A>G NP_001269529.1:p.=
NM_001320810.2:c.-49+5971A>G NP_001307739.1:p.=
NM_004389.4:c.1057-81917A>G NP_004380.2:p.=