Canonical Allele Identifier: CA2592214785

Gene: CTNND2

Linked Data

• gnomAD v3: 5-11385173-C-CGGG
• gnomAD v4: 5-11385173-C-CGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11385175_11385176insGGG , CM000667.2:g.11385175_11385176insGGG	GRCh38
NC_000005.9:g.11385287_11385288insGGG , CM000667.1:g.11385287_11385288insGGG	GRCh37
NC_000005.8:g.11438287_11438288insGGG	NCBI36
NG_023544.1:g.523825_523826insCCC
NG_023544.2:g.523825_523826insCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-20284_167-20283insCCC	ENSP00000516315.1:n.167-20284_167-20283insCCC
ENST00000304623.13:c.668_669insCCC MANE Select	ENSP00000307134.8:p.Pro223_Pro224insPro
ENST00000304623.12:c.668_669insCCC	ENSP00000307134.8:p.Pro223_Pro224insPro
ENST00000502551.5:c.398-20284_398-20283insCCC	ENSP00000422389.1:n.398-20284_398-20283insCCC
ENST00000503622.5:c.167-20284_167-20283insCCC	ENSP00000426887.1:n.167-20284_167-20283insCCC
ENST00000504354.5:n.217-20284_217-20283insCCC
ENST00000504499.5:c.612+11857_612+11858insCCC	ENSP00000421000.1:n.612+11857_612+11858insCCC
ENST00000511278.5:n.542-20284_542-20283insCCC
ENST00000511377.5:c.395_396insCCC	ENSP00000426510.1:p.Pro132_Pro133insPro
ENST00000513588.5:c.440-20284_440-20283insCCC	ENSP00000421093.1:n.440-20284_440-20283insCCC
ENST00000513598.5:c.395_396insCCC	ENSP00000426625.1:p.Pro132_Pro133insPro
ENST00000514132.1:n.317_318insCCC
NM_001288715.1:c.395_396insCCC	NP_001275644.1:p.Pro132_Pro133insPro
NM_001288716.1:c.167-20284_167-20283insCCC	NP_001275645.1:n.167-20284_167-20283insCCC
NM_001288717.1:c.-123+11857_-123+11858insCCC	NP_001275646.1:n.-123+11857_-123+11858insCCC
NM_001332.3:c.668_669insCCC	NP_001323.1:p.Pro223_Pro224insPro
NR_109988.1:n.630-20284_630-20283insCCC
XM_005248251.2:c.668_669insCCC	XP_005248308.1:p.Pro223_Pro224insPro
XM_005248252.1:c.626_627insCCC	XP_005248309.1:p.Pro209_Pro210insPro
XM_005248253.1:c.395_396insCCC	XP_005248310.1:p.Pro132_Pro133insPro
XM_011513967.1:c.395_396insCCC	XP_011512269.1:p.Pro132_Pro133insPro
NM_001364128.1:c.167-20284_167-20283insCCC	NP_001351057.1:n.167-20284_167-20283insCCC
XM_005248251.3:c.668_669insCCC	XP_005248308.1:p.Pro223_Pro224insPro
XM_005248252.2:c.626_627insCCC	XP_005248309.1:p.Pro209_Pro210insPro
XM_011513967.2:c.395_396insCCC	XP_011512269.1:p.Pro132_Pro133insPro
XM_017009072.1:c.440-20284_440-20283insCCC	XP_016864561.1:n.440-20284_440-20283insCCC
XM_017009073.1:c.398-20284_398-20283insCCC	XP_016864562.1:n.398-20284_398-20283insCCC
XM_017009074.1:c.440-20284_440-20283insCCC	XP_016864563.1:n.440-20284_440-20283insCCC
XM_017009075.2:c.167-20284_167-20283insCCC	XP_016864564.1:n.167-20284_167-20283insCCC
NM_001332.4:c.668_669insCCC MANE Select	NP_001323.1:p.Pro223_Pro224insPro
NM_001288717.2:c.-123+11857_-123+11858insCCC	NP_001275646.1:n.-123+11857_-123+11858insCCC
NR_109988.2:n.1033-20284_1033-20283insCCC
NM_001364128.2:c.167-20284_167-20283insCCC	NP_001351057.1:n.167-20284_167-20283insCCC