Canonical Allele Identifier: CA1264345506

Gene: CTNNA2

Linked Data

• dbSNP Id: rs1677559494

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.80311321_80311323del , CM000664.2:g.80311321_80311323del	GRCh38
NC_000002.11:g.80538446_80538448del , CM000664.1:g.80538446_80538448del	GRCh37
NC_000002.10:g.80391957_80391959del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000402739.9:c.1057-81890_1057-81888del MANE Select	ENSP00000384638.4:n.1057-81890_1057-81888...
ENST00000402739.8:c.1057-81890_1057-81888del	ENSP00000384638.4:n.1057-81890_1057-81888...
ENST00000466387.5:c.1057-81890_1057-81888del	ENSP00000418191.1:n.1057-81890_1057-81888...
ENST00000493024.5:n.206+5998_206+6000del
ENST00000496558.5:c.1057-81890_1057-81888del	ENSP00000419295.1:n.1057-81890_1057-81888...
ENST00000541047.5:c.-49+5998_-49+6000del	ENSP00000444675.2:n.-49+5998_-49+6000del
ENST00000629316.2:c.1057-81890_1057-81888del	ENSP00000486160.1:n.1057-81890_1057-81888...
NM_001164883.1:c.1057-81890_1057-81888del	NP_001158355.1:n.1057-81890_1057-81888del...
NM_001282597.2:c.1057-81890_1057-81888del	NP_001269526.1:n.1057-81890_1057-81888del...
NM_001282598.1:c.1159-81890_1159-81888del	NP_001269527.1:n.1159-81890_1159-81888del...
NM_001282600.1:c.-49+5998_-49+6000del	NP_001269529.1:n.-49+5998_-49+6000del
NM_004389.3:c.1057-81890_1057-81888del	NP_004380.2:n.1057-81890_1057-81888del
XM_006711949.2:c.-49+5998_-49+6000del	XP_006712012.1:n.-49+5998_-49+6000del
XM_011532555.1:c.1057-81890_1057-81888del	XP_011530857.1:n.1057-81890_1057-81888del...
XM_011532556.1:c.1057-81890_1057-81888del	XP_011530858.1:n.1057-81890_1057-81888del...
NM_001320810.1:c.-49+5998_-49+6000del	NP_001307739.1:n.-49+5998_-49+6000del
XM_011532555.2:c.1057-81890_1057-81888del	XP_011530857.1:n.1057-81890_1057-81888del...
XM_011532556.2:c.1057-81890_1057-81888del	XP_011530858.1:n.1057-81890_1057-81888del...
XM_017003403.2:c.1057-81890_1057-81888del	XP_016858892.1:n.1057-81890_1057-81888del...
XM_017003404.2:c.1057-81890_1057-81888del	XP_016858893.1:n.1057-81890_1057-81888del...
XM_017003405.2:c.1057-81890_1057-81888del	XP_016858894.1:n.1057-81890_1057-81888del...
XM_017003406.2:c.-49+5998_-49+6000del	XP_016858895.1:n.-49+5998_-49+6000del
XM_024452714.1:c.1057-81890_1057-81888del	XP_024308482.1:n.1057-81890_1057-81888del...
XM_024452715.1:c.1057-81890_1057-81888del	XP_024308483.1:n.1057-81890_1057-81888del...
XM_024452716.1:c.1057-81890_1057-81888del	XP_024308484.1:n.1057-81890_1057-81888del...
NM_001164883.2:c.1057-81890_1057-81888del	NP_001158355.1:n.1057-81890_1057-81888del...
NM_001282597.3:c.1057-81890_1057-81888del MANE Select	NP_001269526.1:n.1057-81890_1057-81888del...
NM_001282598.2:c.1159-81890_1159-81888del	NP_001269527.1:n.1159-81890_1159-81888del...
NM_001282600.2:c.-49+5998_-49+6000del	NP_001269529.1:n.-49+5998_-49+6000del
NM_001320810.2:c.-49+5998_-49+6000del	NP_001307739.1:n.-49+5998_-49+6000del
NM_004389.4:c.1057-81890_1057-81888del	NP_004380.2:n.1057-81890_1057-81888del
NM_001399737.1:c.1057-81890_1057-81888del	NP_001386666.1:n.1057-81890_1057-81888del...