Canonical Allele Identifier: CA2673260074

Gene: CTNND2

Linked Data

• gnomAD v4: 5-11385100-C-CGGT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11385102_11385103insTGG , CM000667.2:g.11385102_11385103insTGG	GRCh38
NC_000005.9:g.11385214_11385215insTGG , CM000667.1:g.11385214_11385215insTGG	GRCh37
NC_000005.8:g.11438214_11438215insTGG	NCBI36
NG_023544.1:g.523898_523899insACC
NG_023544.2:g.523898_523899insACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-20211_167-20210insACC	ENSP00000516315.1:n.167-20211_167-20210insACC
ENST00000304623.13:c.741_742insACC MANE Select	ENSP00000307134.8:p.Ala247_Ala248insThr
ENST00000304623.12:c.741_742insACC	ENSP00000307134.8:p.Ala247_Ala248insThr
ENST00000502551.5:c.398-20211_398-20210insACC	ENSP00000422389.1:n.398-20211_398-20210insACC
ENST00000503622.5:c.167-20211_167-20210insACC	ENSP00000426887.1:n.167-20211_167-20210insACC
ENST00000504354.5:n.217-20211_217-20210insACC
ENST00000504499.5:c.612+11930_612+11931insACC	ENSP00000421000.1:n.612+11930_612+11931insACC
ENST00000511278.5:n.542-20211_542-20210insACC
ENST00000511377.5:c.468_469insACC	ENSP00000426510.1:p.Ala156_Ala157insThr
ENST00000513588.5:c.440-20211_440-20210insACC	ENSP00000421093.1:n.440-20211_440-20210insACC
ENST00000513598.5:c.468_469insACC	ENSP00000426625.1:p.Ala156_Ala157insThr
ENST00000514132.1:n.390_391insACC
NM_001288715.1:c.468_469insACC	NP_001275644.1:p.Ala156_Ala157insThr
NM_001288716.1:c.167-20211_167-20210insACC	NP_001275645.1:n.167-20211_167-20210insACC
NM_001288717.1:c.-123+11930_-123+11931insACC	NP_001275646.1:n.-123+11930_-123+11931insACC
NM_001332.3:c.741_742insACC	NP_001323.1:p.Ala247_Ala248insThr
NR_109988.1:n.630-20211_630-20210insACC
XM_005248251.2:c.741_742insACC	XP_005248308.1:p.Ala247_Ala248insThr
XM_005248252.1:c.699_700insACC	XP_005248309.1:p.Ala233_Ala234insThr
XM_005248253.1:c.468_469insACC	XP_005248310.1:p.Ala156_Ala157insThr
XM_011513967.1:c.468_469insACC	XP_011512269.1:p.Ala156_Ala157insThr
NM_001364128.1:c.167-20211_167-20210insACC	NP_001351057.1:n.167-20211_167-20210insACC
XM_005248251.3:c.741_742insACC	XP_005248308.1:p.Ala247_Ala248insThr
XM_005248252.2:c.699_700insACC	XP_005248309.1:p.Ala233_Ala234insThr
XM_011513967.2:c.468_469insACC	XP_011512269.1:p.Ala156_Ala157insThr
XM_017009072.1:c.440-20211_440-20210insACC	XP_016864561.1:n.440-20211_440-20210insACC
XM_017009073.1:c.398-20211_398-20210insACC	XP_016864562.1:n.398-20211_398-20210insACC
XM_017009074.1:c.440-20211_440-20210insACC	XP_016864563.1:n.440-20211_440-20210insACC
XM_017009075.2:c.167-20211_167-20210insACC	XP_016864564.1:n.167-20211_167-20210insACC
NM_001332.4:c.741_742insACC MANE Select	NP_001323.1:p.Ala247_Ala248insThr
NM_001288717.2:c.-123+11930_-123+11931insACC	NP_001275646.1:n.-123+11930_-123+11931insACC
NR_109988.2:n.1033-20211_1033-20210insACC
NM_001364128.2:c.167-20211_167-20210insACC	NP_001351057.1:n.167-20211_167-20210insACC