Canonical Allele Identifier: CA2673260078

Gene: CTNND2

Linked Data

• gnomAD v4: 5-11385102-GCGGCGGGCGGCGCGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11385106_11385120del , CM000667.2:g.11385106_11385120del	GRCh38
NC_000005.9:g.11385218_11385232del , CM000667.1:g.11385218_11385232del	GRCh37
NC_000005.8:g.11438218_11438232del	NCBI36
NG_023544.1:g.523882_523896del
NG_023544.2:g.523882_523896del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-20227_167-20213del	ENSP00000516315.1:n.167-20227_167-20213del
ENST00000304623.13:c.725_739del MANE Select	ENSP00000307134.8:p.Asp242_Ala246del
ENST00000304623.12:c.725_739del	ENSP00000307134.8:p.Asp242_Ala246del
ENST00000502551.5:c.398-20227_398-20213del	ENSP00000422389.1:n.398-20227_398-20213del
ENST00000503622.5:c.167-20227_167-20213del	ENSP00000426887.1:n.167-20227_167-20213del
ENST00000504354.5:n.217-20227_217-20213del
ENST00000504499.5:c.612+11914_612+11928del	ENSP00000421000.1:n.612+11914_612+11928del
ENST00000511278.5:n.542-20227_542-20213del
ENST00000511377.5:c.452_466del	ENSP00000426510.1:p.Asp151_Ala155del
ENST00000513588.5:c.440-20227_440-20213del	ENSP00000421093.1:n.440-20227_440-20213del
ENST00000513598.5:c.452_466del	ENSP00000426625.1:p.Asp151_Ala155del
ENST00000514132.1:n.374_388del
NM_001288715.1:c.452_466del	NP_001275644.1:p.Asp151_Ala155del
NM_001288716.1:c.167-20227_167-20213del	NP_001275645.1:n.167-20227_167-20213del
NM_001288717.1:c.-123+11914_-123+11928del	NP_001275646.1:n.-123+11914_-123+11928del
NM_001332.3:c.725_739del	NP_001323.1:p.Asp242_Ala246del
NR_109988.1:n.630-20227_630-20213del
XM_005248251.2:c.725_739del	XP_005248308.1:p.Asp242_Ala246del
XM_005248252.1:c.683_697del	XP_005248309.1:p.Asp228_Ala232del
XM_005248253.1:c.452_466del	XP_005248310.1:p.Asp151_Ala155del
XM_011513967.1:c.452_466del	XP_011512269.1:p.Asp151_Ala155del
NM_001364128.1:c.167-20227_167-20213del	NP_001351057.1:n.167-20227_167-20213del
XM_005248251.3:c.725_739del	XP_005248308.1:p.Asp242_Ala246del
XM_005248252.2:c.683_697del	XP_005248309.1:p.Asp228_Ala232del
XM_011513967.2:c.452_466del	XP_011512269.1:p.Asp151_Ala155del
XM_017009072.1:c.440-20227_440-20213del	XP_016864561.1:n.440-20227_440-20213del
XM_017009073.1:c.398-20227_398-20213del	XP_016864562.1:n.398-20227_398-20213del
XM_017009074.1:c.440-20227_440-20213del	XP_016864563.1:n.440-20227_440-20213del
XM_017009075.2:c.167-20227_167-20213del	XP_016864564.1:n.167-20227_167-20213del
NM_001332.4:c.725_739del MANE Select	NP_001323.1:p.Asp242_Ala246del
NM_001288717.2:c.-123+11914_-123+11928del	NP_001275646.1:n.-123+11914_-123+11928del
NR_109988.2:n.1033-20227_1033-20213del
NM_001364128.2:c.167-20227_167-20213del	NP_001351057.1:n.167-20227_167-20213del