Canonical Allele Identifier: CA197715

Gene: CDH1

Linked Data

• ClinVar Variation Id: 187464
• ClinVar RCV Id: RCV000167195 ; RCV000204049 ; RCV000484305
• dbSNP Id: rs786203752
• gnomAD v4: 16-68829784-AT-A
• MyVariant Identifiers: chr16:g.68863691del (hg19) ; chr16:g.68829788del (hg38)
• PubMed: PMID:17545690 ; PMID:24366306 ; PMID:26182300
• ERepo: CA197715/MONDO:0007648/007 ; CA197715/MONDO:0100488/007

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68829788del , CM000678.2:g.68829788del	GRCh38
NC_000016.9:g.68863691del , CM000678.1:g.68863691del	GRCh37
NC_000016.8:g.67421192del	NCBI36
NG_008021.1:g.97497del , LRG_301:g.97497del

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.2430del MANE Select	ENSP00000261769.4:p.Phe810LeufsTer6
ENST00000261769.9:c.2430del	ENSP00000261769.4:p.Phe810LeufsTer6
ENST00000422392.6:c.2247del	ENSP00000414946.2:p.Phe749LeufsTer6
ENST00000562118.1:n.648del
ENST00000562836.5:n.2501del
ENST00000566510.5:c.*1096del	ENSP00000458139.1:n.*1096del
ENST00000566612.5:c.*670del	ENSP00000454782.1:n.*670del
ENST00000611625.4:c.2493del	ENSP00000481063.1:p.Phe831LeufsTer6
ENST00000612417.4:c.1853+3234del	ENSP00000478360.1:n.1853+3234del
ENST00000621016.4:c.1866-4415del	ENSP00000480664.1:n.1866-4415del
NM_004360.3:c.2430del , LRG_301t1:c.2430del	NP_004351.1:p.Phe810LeufsTer6
XM_011523488.1:c.1695del	XP_011521790.1:p.Phe565LeufsTer6
XM_011523489.1:c.1695del	XP_011521791.1:p.Phe565LeufsTer6
NM_001317184.1:c.2247del	NP_001304113.1:p.Phe749LeufsTer6
NM_001317185.1:c.882del	NP_001304114.1:p.Phe294LeufsTer6
NM_001317186.1:c.465del	NP_001304115.1:p.Phe155LeufsTer6
NM_004360.4:c.2430del	NP_004351.1:p.Phe810LeufsTer6
NM_004360.5:c.2430del MANE Select	NP_004351.1:p.Phe810LeufsTer6
NM_001317184.2:c.2247del	NP_001304113.1:p.Phe749LeufsTer6
NM_001317185.2:c.882del	NP_001304114.1:p.Phe294LeufsTer6
NM_001317186.2:c.465del	NP_001304115.1:p.Phe155LeufsTer6