Canonical Allele Identifier: CA51171466

Gene: CTNNA2

Linked Data

• dbSNP Id: rs1007371
• gnomAD v2: 2-80553345-T-A
• gnomAD v3: 2-80326220-T-A
• gnomAD v4: 2-80326220-T-A
• MyVariant Identifiers: chr2:g.80553345T>A (hg19) ; chr2:g.80326220T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.80326220T>A , CM000664.2:g.80326220T>A	GRCh38
NC_000002.11:g.80553345T>A , CM000664.1:g.80553345T>A	GRCh37
NC_000002.10:g.80406856T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000402739.9:c.1057-66991T>A MANE Select	ENSP00000384638.4:n.1057-66991T>A
ENST00000343114.7:c.93+12566T>A	ENSP00000341500.3:n.93+12566T>A
ENST00000361291.8:c.-97+12566T>A	ENSP00000355398.5:n.-97+12566T>A
ENST00000402739.8:c.1057-66991T>A	ENSP00000384638.4:n.1057-66991T>A
ENST00000466387.5:c.1057-66991T>A	ENSP00000418191.1:n.1057-66991T>A
ENST00000493024.5:n.206+20897T>A
ENST00000496558.5:c.1057-66991T>A	ENSP00000419295.1:n.1057-66991T>A
ENST00000540488.5:c.-97+12566T>A	ENSP00000441705.2:n.-97+12566T>A
ENST00000541047.5:c.-49+20897T>A	ENSP00000444675.2:n.-49+20897T>A
ENST00000629316.2:c.1057-66991T>A	ENSP00000486160.1:n.1057-66991T>A
NM_001164883.1:c.1057-66991T>A	NP_001158355.1:n.1057-66991T>A
NM_001282597.2:c.1057-66991T>A	NP_001269526.1:n.1057-66991T>A
NM_001282598.1:c.1159-66991T>A	NP_001269527.1:n.1159-66991T>A
NM_001282599.1:c.93+12566T>A	NP_001269528.1:n.93+12566T>A
NM_001282600.1:c.-49+20897T>A	NP_001269529.1:n.-49+20897T>A
NM_004389.3:c.1057-66991T>A	NP_004380.2:n.1057-66991T>A
XM_006711949.2:c.-49+20897T>A	XP_006712012.1:n.-49+20897T>A
XM_011532555.1:c.1057-66991T>A	XP_011530857.1:n.1057-66991T>A
XM_011532556.1:c.1057-66991T>A	XP_011530858.1:n.1057-66991T>A
NM_001320810.1:c.-49+20897T>A	NP_001307739.1:n.-49+20897T>A
XM_011532555.2:c.1057-66991T>A	XP_011530857.1:n.1057-66991T>A
XM_011532556.2:c.1057-66991T>A	XP_011530858.1:n.1057-66991T>A
XM_017003403.2:c.1057-66991T>A	XP_016858892.1:n.1057-66991T>A
XM_017003404.2:c.1057-66991T>A	XP_016858893.1:n.1057-66991T>A
XM_017003405.2:c.1057-66991T>A	XP_016858894.1:n.1057-66991T>A
XM_017003406.2:c.-49+20897T>A	XP_016858895.1:n.-49+20897T>A
XM_024452714.1:c.1057-66991T>A	XP_024308482.1:n.1057-66991T>A
XM_024452715.1:c.1057-66991T>A	XP_024308483.1:n.1057-66991T>A
XM_024452716.1:c.1057-66991T>A	XP_024308484.1:n.1057-66991T>A
XR_001739570.1:n.311-813T>A
NM_001164883.2:c.1057-66991T>A	NP_001158355.1:n.1057-66991T>A
NM_001282597.3:c.1057-66991T>A MANE Select	NP_001269526.1:n.1057-66991T>A
NM_001282598.2:c.1159-66991T>A	NP_001269527.1:n.1159-66991T>A
NM_001282599.2:c.93+12566T>A	NP_001269528.1:n.93+12566T>A
NM_001282600.2:c.-49+20897T>A	NP_001269529.1:n.-49+20897T>A
NM_001320810.2:c.-49+20897T>A	NP_001307739.1:n.-49+20897T>A
NM_004389.4:c.1057-66991T>A	NP_004380.2:n.1057-66991T>A
NM_001399737.1:c.1057-66991T>A	NP_001386666.1:n.1057-66991T>A