Canonical Allele Identifier: CA916081837

Gene: CDH1

Linked Data

• ClinVar Variation Id: 856609
• ClinVar RCV Id: RCV001062108 ; RCV002418526
• dbSNP Id: rs1960785108

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68810309_68810319del , CM000678.2:g.68810309_68810319del	GRCh38
NC_000016.9:g.68844212_68844222del , CM000678.1:g.68844212_68844222del	GRCh37
NC_000016.8:g.67401713_67401723del	NCBI36
NG_008021.1:g.78018_78028del , LRG_301:g.78018_78028del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.800_810del MANE Select	ENSP00000261769.4:p.Phe267CysfsTer22
ENST00000261769.9:c.800_810del	ENSP00000261769.4:p.Phe267CysfsTer22
ENST00000422392.6:c.800_810del	ENSP00000414946.2:p.Phe267CysfsTer22
ENST00000561751.1:c.455-1375_455-1365del
ENST00000562836.5:n.871_881del
ENST00000566510.5:c.644_654del	ENSP00000458139.1:p.Phe215CysfsTer22
ENST00000566612.5:c.800_810del	ENSP00000454782.1:p.Phe267CysfsTer22
ENST00000611625.4:c.800_810del	ENSP00000481063.1:p.Phe267CysfsTer22
ENST00000612417.4:c.800_810del	ENSP00000478360.1:p.Phe267CysfsTer22
ENST00000621016.4:c.800_810del	ENSP00000480664.1:p.Phe267CysfsTer22
NM_004360.3:c.800_810del , LRG_301t1:c.800_810del	NP_004351.1:p.Phe267CysfsTer22
XM_011523488.1:c.65_75del	XP_011521790.1:p.Phe22CysfsTer22
XM_011523489.1:c.65_75del	XP_011521791.1:p.Phe22CysfsTer22
NM_001317184.1:c.800_810del	NP_001304113.1:p.Phe267CysfsTer22
NM_001317185.1:c.-816_-806del	NP_001304114.1:n.-816_-806del
NM_001317186.1:c.-1020_-1010del	NP_001304115.1:n.-1020_-1010del
NM_004360.4:c.800_810del	NP_004351.1:p.Phe267CysfsTer22
NM_004360.5:c.800_810del MANE Select	NP_004351.1:p.Phe267CysfsTer22
NM_001317184.2:c.800_810del	NP_001304113.1:p.Phe267CysfsTer22
NM_001317185.2:c.-816_-806del	NP_001304114.1:n.-816_-806del
NM_001317186.2:c.-1020_-1010del	NP_001304115.1:n.-1020_-1010del