Canonical Allele Identifier: CA1264044639

Gene: CTNNA2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.79695676C>A , CM000664.2:g.79695676C>A	GRCh38
NC_000002.11:g.79922802C>A , CM000664.1:g.79922802C>A	GRCh37
NC_000002.10:g.79776310C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402739.9:c.102+44018C>A MANE Select	ENSP00000384638.4:n.102+44018C>A
ENST00000402739.8:c.102+44018C>A	ENSP00000384638.4:n.102+44018C>A
ENST00000409971.6:c.102+44018C>A	ENSP00000387073.2:n.102+44018C>A
ENST00000451966.5:c.102+44018C>A	ENSP00000400105.1:n.102+44018C>A
ENST00000466387.5:c.102+44018C>A	ENSP00000418191.1:n.102+44018C>A
ENST00000496558.5:c.102+44018C>A	ENSP00000419295.1:n.102+44018C>A
ENST00000629316.2:c.102+44018C>A	ENSP00000486160.1:n.102+44018C>A
NM_001164883.1:c.102+44018C>A	NP_001158355.1:n.102+44018C>A
NM_001282597.2:c.102+44018C>A	NP_001269526.1:n.102+44018C>A
NM_001282598.1:c.204+44018C>A	NP_001269527.1:n.204+44018C>A
NM_004389.3:c.102+44018C>A	NP_004380.2:n.102+44018C>A
XM_011532555.1:c.102+44018C>A	XP_011530857.1:n.102+44018C>A
XM_011532556.1:c.102+44018C>A	XP_011530858.1:n.102+44018C>A
XM_011532555.2:c.102+44018C>A	XP_011530857.1:n.102+44018C>A
XM_011532556.2:c.102+44018C>A	XP_011530858.1:n.102+44018C>A
XM_017003403.2:c.102+44018C>A	XP_016858892.1:n.102+44018C>A
XM_017003404.2:c.102+44018C>A	XP_016858893.1:n.102+44018C>A
XM_017003405.2:c.102+44018C>A	XP_016858894.1:n.102+44018C>A
XM_024452714.1:c.102+44018C>A	XP_024308482.1:n.102+44018C>A
XM_024452715.1:c.102+44018C>A	XP_024308483.1:n.102+44018C>A
XM_024452716.1:c.102+44018C>A	XP_024308484.1:n.102+44018C>A
NM_001164883.2:c.102+44018C>A	NP_001158355.1:n.102+44018C>A
NM_001282597.3:c.102+44018C>A MANE Select	NP_001269526.1:n.102+44018C>A
NM_001282598.2:c.204+44018C>A	NP_001269527.1:n.204+44018C>A
NM_004389.4:c.102+44018C>A	NP_004380.2:n.102+44018C>A
NM_001399737.1:c.102+44018C>A	NP_001386666.1:n.102+44018C>A