Canonical Allele Identifier: CA283319803
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2874464
ClinVar RCV Id: RCV003623983
dbSNP Id: rs869090510
MyVariant Identifiers: chr16:g.68867402del (hg19) chr16:g.68833499del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833502del , CM000678.2:g.68833502del GRCh38
NC_000016.9:g.68867405del , CM000678.1:g.68867405del GRCh37
NC_000016.8:g.67424906del NCBI36
NG_008021.1:g.101211del , LRG_301:g.101211del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.*3del MANE Select ENSP00000261769.4:n.*3del
ENST00000261769.9:c.*3del ENSP00000261769.4:n.*3del
ENST00000422392.6:c.*3del ENSP00000414946.2:n.*3del
ENST00000562118.1:n.870del
ENST00000562836.5:n.2723del
ENST00000566510.5:c.*1318del ENSP00000458139.1:n.*1318del
ENST00000566612.5:c.*892del ENSP00000454782.1:n.*892del
ENST00000611625.4:c.*3del ENSP00000481063.1:n.*3del
ENST00000612417.4:c.1854-689del ENSP00000478360.1:n.1854-689del
ENST00000621016.4:c.1866-701del ENSP00000480664.1:n.1866-701del
NM_004360.3:c.*3del , LRG_301t1:c.*3del NP_004351.1:n.*3del
XM_011523488.1:c.*3del XP_011521790.1:n.*3del
XM_011523489.1:c.*3del XP_011521791.1:n.*3del
NM_001317184.1:c.*3del NP_001304113.1:n.*3del
NM_001317185.1:c.*3del NP_001304114.1:n.*3del
NM_001317186.1:c.*3del NP_001304115.1:n.*3del
NM_004360.4:c.*3del NP_004351.1:n.*3del
NM_004360.5:c.*3del MANE Select NP_004351.1:n.*3del
NM_001317184.2:c.*3del NP_001304113.1:n.*3del
NM_001317185.2:c.*3del NP_001304114.1:n.*3del
NM_001317186.2:c.*3del NP_001304115.1:n.*3del
Search 100 bp 5'
Search 100 bp 3'