Canonical Allele Identifier: CA2592214783

Gene: CTNND2

Linked Data

• gnomAD v3: 5-11385162-C-CGCGGCGGCGGCGGCG
• gnomAD v4: 5-11385162-C-CGCGGCGGCGGCGGCG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11385172_11385186dup , CM000667.2:g.11385172_11385186dup	GRCh38
NC_000005.9:g.11385284_11385298dup , CM000667.1:g.11385284_11385298dup	GRCh37
NC_000005.8:g.11438284_11438298dup	NCBI36
NG_023544.1:g.523822_523836dup
NG_023544.2:g.523822_523836dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-20287_167-20273dup	ENSP00000516315.1:n.167-20287_167-20273dup
ENST00000304623.13:c.665_679dup MANE Select	ENSP00000307134.8:p.Pro226_Arg227insProProProProPro
ENST00000304623.12:c.665_679dup	ENSP00000307134.8:p.Pro226_Arg227insProProProProPro
ENST00000502551.5:c.398-20287_398-20273dup	ENSP00000422389.1:n.398-20287_398-20273dup
ENST00000503622.5:c.167-20287_167-20273dup	ENSP00000426887.1:n.167-20287_167-20273dup
ENST00000504354.5:n.217-20287_217-20273dup
ENST00000504499.5:c.612+11854_612+11868dup	ENSP00000421000.1:n.612+11854_612+11868dup
ENST00000511278.5:n.542-20287_542-20273dup
ENST00000511377.5:c.392_406dup	ENSP00000426510.1:p.Pro135_Arg136insProProProProPro
ENST00000513588.5:c.440-20287_440-20273dup	ENSP00000421093.1:n.440-20287_440-20273dup
ENST00000513598.5:c.392_406dup	ENSP00000426625.1:p.Pro135_Arg136insProProProProPro
ENST00000514132.1:n.314_328dup
NM_001288715.1:c.392_406dup	NP_001275644.1:p.Pro135_Arg136insProProProProPro
NM_001288716.1:c.167-20287_167-20273dup	NP_001275645.1:n.167-20287_167-20273dup
NM_001288717.1:c.-123+11854_-123+11868dup	NP_001275646.1:n.-123+11854_-123+11868dup
NM_001332.3:c.665_679dup	NP_001323.1:p.Pro226_Arg227insProProProProPro
NR_109988.1:n.630-20287_630-20273dup
XM_005248251.2:c.665_679dup	XP_005248308.1:p.Pro226_Arg227insProProProProPro
XM_005248252.1:c.623_637dup	XP_005248309.1:p.Pro212_Arg213insProProProProPro
XM_005248253.1:c.392_406dup	XP_005248310.1:p.Pro135_Arg136insProProProProPro
XM_011513967.1:c.392_406dup	XP_011512269.1:p.Pro135_Arg136insProProProProPro
NM_001364128.1:c.167-20287_167-20273dup	NP_001351057.1:n.167-20287_167-20273dup
XM_005248251.3:c.665_679dup	XP_005248308.1:p.Pro226_Arg227insProProProProPro
XM_005248252.2:c.623_637dup	XP_005248309.1:p.Pro212_Arg213insProProProProPro
XM_011513967.2:c.392_406dup	XP_011512269.1:p.Pro135_Arg136insProProProProPro
XM_017009072.1:c.440-20287_440-20273dup	XP_016864561.1:n.440-20287_440-20273dup
XM_017009073.1:c.398-20287_398-20273dup	XP_016864562.1:n.398-20287_398-20273dup
XM_017009074.1:c.440-20287_440-20273dup	XP_016864563.1:n.440-20287_440-20273dup
XM_017009075.2:c.167-20287_167-20273dup	XP_016864564.1:n.167-20287_167-20273dup
NM_001332.4:c.665_679dup MANE Select	NP_001323.1:p.Pro226_Arg227insProProProProPro
NM_001288717.2:c.-123+11854_-123+11868dup	NP_001275646.1:n.-123+11854_-123+11868dup
NR_109988.2:n.1033-20287_1033-20273dup
NM_001364128.2:c.167-20287_167-20273dup	NP_001351057.1:n.167-20287_167-20273dup