Canonical Allele Identifier: CA16103863

Gene: CTNNA2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.80054047A>G , CM000664.2:g.80054047A>G	GRCh38
NC_000002.11:g.80281173A>G , CM000664.1:g.80281173A>G	GRCh37
NC_000002.10:g.80134684A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402739.9:c.1056+144250A>G MANE Select	ENSP00000384638.4:n.1056+144250A>G
ENST00000402739.8:c.1056+144250A>G	ENSP00000384638.4:n.1056+144250A>G
ENST00000466387.5:c.1056+144250A>G	ENSP00000418191.1:n.1056+144250A>G
ENST00000496558.5:c.1056+144250A>G	ENSP00000419295.1:n.1056+144250A>G
ENST00000629316.2:c.1056+144250A>G	ENSP00000486160.1:n.1056+144250A>G
NM_001164883.1:c.1056+144250A>G	NP_001158355.1:n.1056+144250A>G
NM_001282597.2:c.1056+144250A>G	NP_001269526.1:n.1056+144250A>G
NM_001282598.1:c.1158+144250A>G	NP_001269527.1:n.1158+144250A>G
NM_004389.3:c.1056+144250A>G	NP_004380.2:n.1056+144250A>G
XM_011532555.1:c.1056+144250A>G	XP_011530857.1:n.1056+144250A>G
XM_011532556.1:c.1056+144250A>G	XP_011530858.1:n.1056+144250A>G
XM_011532555.2:c.1056+144250A>G	XP_011530857.1:n.1056+144250A>G
XM_011532556.2:c.1056+144250A>G	XP_011530858.1:n.1056+144250A>G
XM_017003403.2:c.1056+144250A>G	XP_016858892.1:n.1056+144250A>G
XM_017003404.2:c.1056+144250A>G	XP_016858893.1:n.1056+144250A>G
XM_017003405.2:c.1056+144250A>G	XP_016858894.1:n.1056+144250A>G
XM_024452714.1:c.1056+144250A>G	XP_024308482.1:n.1056+144250A>G
XM_024452715.1:c.1056+144250A>G	XP_024308483.1:n.1056+144250A>G
XM_024452716.1:c.1056+144250A>G	XP_024308484.1:n.1056+144250A>G
NM_001164883.2:c.1056+144250A>G	NP_001158355.1:n.1056+144250A>G
NM_001282597.3:c.1056+144250A>G MANE Select	NP_001269526.1:n.1056+144250A>G
NM_001282598.2:c.1158+144250A>G	NP_001269527.1:n.1158+144250A>G
NM_004389.4:c.1056+144250A>G	NP_004380.2:n.1056+144250A>G
NM_001399737.1:c.1056+144250A>G	NP_001386666.1:n.1056+144250A>G