Canonical Allele Identifier: CA2673260097

Gene: CTNND2

Linked Data

• gnomAD v4: 5-11385175-GCGGCGGCGGCGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11385176_11385187del , CM000667.2:g.11385176_11385187del	GRCh38
NC_000005.9:g.11385288_11385299del , CM000667.1:g.11385288_11385299del	GRCh37
NC_000005.8:g.11438288_11438299del	NCBI36
NG_023544.1:g.523812_523823del
NG_023544.2:g.523812_523823del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-20297_167-20286del	ENSP00000516315.1:n.167-20297_167-20286del
ENST00000304623.13:c.655_666del MANE Select	ENSP00000307134.8:p.Ala219_Pro222del
ENST00000304623.12:c.655_666del	ENSP00000307134.8:p.Ala219_Pro222del
ENST00000502551.5:c.398-20297_398-20286del	ENSP00000422389.1:n.398-20297_398-20286del
ENST00000503622.5:c.167-20297_167-20286del	ENSP00000426887.1:n.167-20297_167-20286del
ENST00000504354.5:n.217-20297_217-20286del
ENST00000504499.5:c.612+11844_612+11855del	ENSP00000421000.1:n.612+11844_612+11855del
ENST00000511278.5:n.542-20297_542-20286del
ENST00000511377.5:c.382_393del	ENSP00000426510.1:p.Ala128_Pro131del
ENST00000513588.5:c.440-20297_440-20286del	ENSP00000421093.1:n.440-20297_440-20286del
ENST00000513598.5:c.382_393del	ENSP00000426625.1:p.Ala128_Pro131del
ENST00000514132.1:n.304_315del
NM_001288715.1:c.382_393del	NP_001275644.1:p.Ala128_Pro131del
NM_001288716.1:c.167-20297_167-20286del	NP_001275645.1:n.167-20297_167-20286del
NM_001288717.1:c.-123+11844_-123+11855del	NP_001275646.1:n.-123+11844_-123+11855del
NM_001332.3:c.655_666del	NP_001323.1:p.Ala219_Pro222del
NR_109988.1:n.630-20297_630-20286del
XM_005248251.2:c.655_666del	XP_005248308.1:p.Ala219_Pro222del
XM_005248252.1:c.613_624del	XP_005248309.1:p.Ala205_Pro208del
XM_005248253.1:c.382_393del	XP_005248310.1:p.Ala128_Pro131del
XM_011513967.1:c.382_393del	XP_011512269.1:p.Ala128_Pro131del
NM_001364128.1:c.167-20297_167-20286del	NP_001351057.1:n.167-20297_167-20286del
XM_005248251.3:c.655_666del	XP_005248308.1:p.Ala219_Pro222del
XM_005248252.2:c.613_624del	XP_005248309.1:p.Ala205_Pro208del
XM_011513967.2:c.382_393del	XP_011512269.1:p.Ala128_Pro131del
XM_017009072.1:c.440-20297_440-20286del	XP_016864561.1:n.440-20297_440-20286del
XM_017009073.1:c.398-20297_398-20286del	XP_016864562.1:n.398-20297_398-20286del
XM_017009074.1:c.440-20297_440-20286del	XP_016864563.1:n.440-20297_440-20286del
XM_017009075.2:c.167-20297_167-20286del	XP_016864564.1:n.167-20297_167-20286del
NM_001332.4:c.655_666del MANE Select	NP_001323.1:p.Ala219_Pro222del
NM_001288717.2:c.-123+11844_-123+11855del	NP_001275646.1:n.-123+11844_-123+11855del
NR_109988.2:n.1033-20297_1033-20286del
NM_001364128.2:c.167-20297_167-20286del	NP_001351057.1:n.167-20297_167-20286del