Canonical Allele Identifier: CA2673260076

Gene: CTNND2

Linked Data

• gnomAD v4: 5-11385102-G-GCGA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11385104_11385105insACG , CM000667.2:g.11385104_11385105insACG	GRCh38
NC_000005.9:g.11385216_11385217insACG , CM000667.1:g.11385216_11385217insACG	GRCh37
NC_000005.8:g.11438216_11438217insACG	NCBI36
NG_023544.1:g.523896_523897insTCG
NG_023544.2:g.523896_523897insTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-20213_167-20212insTCG	ENSP00000516315.1:n.167-20213_167-20212insTCG
ENST00000304623.13:c.739_740insTCG MANE Select	ENSP00000307134.8:p.Ala246_Ala247insVal
ENST00000304623.12:c.739_740insTCG	ENSP00000307134.8:p.Ala246_Ala247insVal
ENST00000502551.5:c.398-20213_398-20212insTCG	ENSP00000422389.1:n.398-20213_398-20212insTCG
ENST00000503622.5:c.167-20213_167-20212insTCG	ENSP00000426887.1:n.167-20213_167-20212insTCG
ENST00000504354.5:n.217-20213_217-20212insTCG
ENST00000504499.5:c.612+11928_612+11929insTCG	ENSP00000421000.1:n.612+11928_612+11929insTCG
ENST00000511278.5:n.542-20213_542-20212insTCG
ENST00000511377.5:c.466_467insTCG	ENSP00000426510.1:p.Ala155_Ala156insVal
ENST00000513588.5:c.440-20213_440-20212insTCG	ENSP00000421093.1:n.440-20213_440-20212insTCG
ENST00000513598.5:c.466_467insTCG	ENSP00000426625.1:p.Ala155_Ala156insVal
ENST00000514132.1:n.388_389insTCG
NM_001288715.1:c.466_467insTCG	NP_001275644.1:p.Ala155_Ala156insVal
NM_001288716.1:c.167-20213_167-20212insTCG	NP_001275645.1:n.167-20213_167-20212insTCG
NM_001288717.1:c.-123+11928_-123+11929insTCG	NP_001275646.1:n.-123+11928_-123+11929insTCG
NM_001332.3:c.739_740insTCG	NP_001323.1:p.Ala246_Ala247insVal
NR_109988.1:n.630-20213_630-20212insTCG
XM_005248251.2:c.739_740insTCG	XP_005248308.1:p.Ala246_Ala247insVal
XM_005248252.1:c.697_698insTCG	XP_005248309.1:p.Ala232_Ala233insVal
XM_005248253.1:c.466_467insTCG	XP_005248310.1:p.Ala155_Ala156insVal
XM_011513967.1:c.466_467insTCG	XP_011512269.1:p.Ala155_Ala156insVal
NM_001364128.1:c.167-20213_167-20212insTCG	NP_001351057.1:n.167-20213_167-20212insTCG
XM_005248251.3:c.739_740insTCG	XP_005248308.1:p.Ala246_Ala247insVal
XM_005248252.2:c.697_698insTCG	XP_005248309.1:p.Ala232_Ala233insVal
XM_011513967.2:c.466_467insTCG	XP_011512269.1:p.Ala155_Ala156insVal
XM_017009072.1:c.440-20213_440-20212insTCG	XP_016864561.1:n.440-20213_440-20212insTCG
XM_017009073.1:c.398-20213_398-20212insTCG	XP_016864562.1:n.398-20213_398-20212insTCG
XM_017009074.1:c.440-20213_440-20212insTCG	XP_016864563.1:n.440-20213_440-20212insTCG
XM_017009075.2:c.167-20213_167-20212insTCG	XP_016864564.1:n.167-20213_167-20212insTCG
NM_001332.4:c.739_740insTCG MANE Select	NP_001323.1:p.Ala246_Ala247insVal
NM_001288717.2:c.-123+11928_-123+11929insTCG	NP_001275646.1:n.-123+11928_-123+11929insTCG
NR_109988.2:n.1033-20213_1033-20212insTCG
NM_001364128.2:c.167-20213_167-20212insTCG	NP_001351057.1:n.167-20213_167-20212insTCG