Canonical Allele Identifier: CA2673260081

Gene: CTNND2

Linked Data

• gnomAD v4: 5-11385103-CGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11385104_11385105del , CM000667.2:g.11385104_11385105del	GRCh38
NC_000005.9:g.11385216_11385217del , CM000667.1:g.11385216_11385217del	GRCh37
NC_000005.8:g.11438216_11438217del	NCBI36
NG_023544.1:g.523894_523895del
NG_023544.2:g.523894_523895del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-20215_167-20214del	ENSP00000516315.1:n.167-20215_167-20214del
ENST00000304623.13:c.737_738del MANE Select	ENSP00000307134.8:p.Ala246GlyfsTer?
ENST00000304623.12:c.737_738del	ENSP00000307134.8:p.Ala246GlyfsTer?
ENST00000502551.5:c.398-20215_398-20214del	ENSP00000422389.1:n.398-20215_398-20214del
ENST00000503622.5:c.167-20215_167-20214del	ENSP00000426887.1:n.167-20215_167-20214del
ENST00000504354.5:n.217-20215_217-20214del
ENST00000504499.5:c.612+11926_612+11927del	ENSP00000421000.1:n.612+11926_612+11927del
ENST00000511278.5:n.542-20215_542-20214del
ENST00000511377.5:c.464_465del	ENSP00000426510.1:p.Ala155GlyfsTer?
ENST00000513588.5:c.440-20215_440-20214del	ENSP00000421093.1:n.440-20215_440-20214del
ENST00000513598.5:c.464_465del	ENSP00000426625.1:p.Ala155GlyfsTer?
ENST00000514132.1:n.386_387del
NM_001288715.1:c.464_465del	NP_001275644.1:p.Ala155GlyfsTer?
NM_001288716.1:c.167-20215_167-20214del	NP_001275645.1:n.167-20215_167-20214del
NM_001288717.1:c.-123+11926_-123+11927del	NP_001275646.1:n.-123+11926_-123+11927del
NM_001332.3:c.737_738del	NP_001323.1:p.Ala246GlyfsTer?
NR_109988.1:n.630-20215_630-20214del
XM_005248251.2:c.737_738del	XP_005248308.1:p.Ala246GlyfsTer?
XM_005248252.1:c.695_696del	XP_005248309.1:p.Ala232GlyfsTer?
XM_005248253.1:c.464_465del	XP_005248310.1:p.Ala155GlyfsTer?
XM_011513967.1:c.464_465del	XP_011512269.1:p.Ala155GlyfsTer?
NM_001364128.1:c.167-20215_167-20214del	NP_001351057.1:n.167-20215_167-20214del
XM_005248251.3:c.737_738del	XP_005248308.1:p.Ala246GlyfsTer?
XM_005248252.2:c.695_696del	XP_005248309.1:p.Ala232GlyfsTer?
XM_011513967.2:c.464_465del	XP_011512269.1:p.Ala155GlyfsTer?
XM_017009072.1:c.440-20215_440-20214del	XP_016864561.1:n.440-20215_440-20214del
XM_017009073.1:c.398-20215_398-20214del	XP_016864562.1:n.398-20215_398-20214del
XM_017009074.1:c.440-20215_440-20214del	XP_016864563.1:n.440-20215_440-20214del
XM_017009075.2:c.167-20215_167-20214del	XP_016864564.1:n.167-20215_167-20214del
NM_001332.4:c.737_738del MANE Select	NP_001323.1:p.Ala246GlyfsTer?
NM_001288717.2:c.-123+11926_-123+11927del	NP_001275646.1:n.-123+11926_-123+11927del
NR_109988.2:n.1033-20215_1033-20214del
NM_001364128.2:c.167-20215_167-20214del	NP_001351057.1:n.167-20215_167-20214del