Canonical Allele Identifier: CA2673260101

Gene: CTNND2

Linked Data

• gnomAD v4: 5-11385186-G-GCGGGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11385192_11385197dup , CM000667.2:g.11385192_11385197dup	GRCh38
NC_000005.9:g.11385304_11385309dup , CM000667.1:g.11385304_11385309dup	GRCh37
NC_000005.8:g.11438304_11438309dup	NCBI36
NG_023544.1:g.523807_523812dup
NG_023544.2:g.523807_523812dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-20302_167-20297dup	ENSP00000516315.1:n.167-20302_167-20297dup
ENST00000304623.13:c.650_655dup MANE Select	ENSP00000307134.8:p.Pro218_Ala219insGluPro
ENST00000304623.12:c.650_655dup	ENSP00000307134.8:p.Pro218_Ala219insGluPro
ENST00000502551.5:c.398-20302_398-20297dup	ENSP00000422389.1:n.398-20302_398-20297dup
ENST00000503622.5:c.167-20302_167-20297dup	ENSP00000426887.1:n.167-20302_167-20297dup
ENST00000504354.5:n.217-20302_217-20297dup
ENST00000504499.5:c.612+11839_612+11844dup	ENSP00000421000.1:n.612+11839_612+11844dup
ENST00000511278.5:n.542-20302_542-20297dup
ENST00000511377.5:c.377_382dup	ENSP00000426510.1:p.Pro127_Ala128insGluPro
ENST00000513588.5:c.440-20302_440-20297dup	ENSP00000421093.1:n.440-20302_440-20297dup
ENST00000513598.5:c.377_382dup	ENSP00000426625.1:p.Pro127_Ala128insGluPro
ENST00000514132.1:n.299_304dup
NM_001288715.1:c.377_382dup	NP_001275644.1:p.Pro127_Ala128insGluPro
NM_001288716.1:c.167-20302_167-20297dup	NP_001275645.1:n.167-20302_167-20297dup
NM_001288717.1:c.-123+11839_-123+11844dup	NP_001275646.1:n.-123+11839_-123+11844dup
NM_001332.3:c.650_655dup	NP_001323.1:p.Pro218_Ala219insGluPro
NR_109988.1:n.630-20302_630-20297dup
XM_005248251.2:c.650_655dup	XP_005248308.1:p.Pro218_Ala219insGluPro
XM_005248252.1:c.608_613dup	XP_005248309.1:p.Pro204_Ala205insGluPro
XM_005248253.1:c.377_382dup	XP_005248310.1:p.Pro127_Ala128insGluPro
XM_011513967.1:c.377_382dup	XP_011512269.1:p.Pro127_Ala128insGluPro
NM_001364128.1:c.167-20302_167-20297dup	NP_001351057.1:n.167-20302_167-20297dup
XM_005248251.3:c.650_655dup	XP_005248308.1:p.Pro218_Ala219insGluPro
XM_005248252.2:c.608_613dup	XP_005248309.1:p.Pro204_Ala205insGluPro
XM_011513967.2:c.377_382dup	XP_011512269.1:p.Pro127_Ala128insGluPro
XM_017009072.1:c.440-20302_440-20297dup	XP_016864561.1:n.440-20302_440-20297dup
XM_017009073.1:c.398-20302_398-20297dup	XP_016864562.1:n.398-20302_398-20297dup
XM_017009074.1:c.440-20302_440-20297dup	XP_016864563.1:n.440-20302_440-20297dup
XM_017009075.2:c.167-20302_167-20297dup	XP_016864564.1:n.167-20302_167-20297dup
NM_001332.4:c.650_655dup MANE Select	NP_001323.1:p.Pro218_Ala219insGluPro
NM_001288717.2:c.-123+11839_-123+11844dup	NP_001275646.1:n.-123+11839_-123+11844dup
NR_109988.2:n.1033-20302_1033-20297dup
NM_001364128.2:c.167-20302_167-20297dup	NP_001351057.1:n.167-20302_167-20297dup