Canonical Allele Identifier: CA2633927835

Gene: CDH3

Linked Data

• gnomAD v4: 16-68680961-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68680965del , CM000678.2:g.68680965del	GRCh38
NC_000016.9:g.68714868del , CM000678.1:g.68714868del	GRCh37
NC_000016.8:g.67272369del	NCBI36
NG_009096.1:g.41718del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264012.9:c.868-3del MANE Select	ENSP00000264012.4:n.868-3del
ENST00000264012.8:c.868-3del	ENSP00000264012.4:n.868-3del
ENST00000429102.6:c.868-3del	ENSP00000398485.2:n.868-3del
ENST00000542274.5:c.*606-3del	ENSP00000464021.1:n.*606-3del
ENST00000569036.2:c.344-3del
NM_001793.4:c.868-3del	NP_001784.2:n.868-3del
XM_011522800.1:c.868-3del	XP_011521102.1:n.868-3del
NM_001317195.1:c.868-3del	NP_001304124.1:n.868-3del
NM_001317196.1:c.703-3del	NP_001304125.1:n.703-3del
NM_001793.5:c.868-3del	NP_001784.2:n.868-3del
XM_011522800.3:c.868-3del	XP_011521102.1:n.868-3del
NM_001793.6:c.868-3del MANE Select	NP_001784.2:n.868-3del
NM_001317195.2:c.868-3del	NP_001304124.1:n.868-3del
NM_001317196.2:c.703-3del	NP_001304125.1:n.703-3del
NM_001317195.3:c.868-3del	NP_001304124.1:n.868-3del