Canonical Allele Identifier: CA2582342555

Gene: CDH1

Linked Data

• ClinVar Variation Id: 2583590
• ClinVar RCV Id: RCV003334512

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68801807_68801820del , CM000678.2:g.68801807_68801820del	GRCh38
NC_000016.9:g.68835710_68835723del , CM000678.1:g.68835710_68835723del	GRCh37
NC_000016.8:g.67393211_67393224del	NCBI36
NG_008021.1:g.69516_69529del , LRG_301:g.69516_69529del

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.301_314del MANE Select	ENSP00000261769.4:p.Tyr101HisfsTer?
ENST00000261769.9:c.301_314del	ENSP00000261769.4:p.Tyr101HisfsTer?
ENST00000422392.6:c.301_314del	ENSP00000414946.2:p.Tyr101HisfsTer?
ENST00000561751.1:c.68_81del
ENST00000562836.5:n.372_385del
ENST00000564676.5:n.583_596del
ENST00000564745.1:n.296_309del
ENST00000566510.5:c.301_314del	ENSP00000458139.1:p.Tyr101HisfsTer?
ENST00000566612.5:c.301_314del	ENSP00000454782.1:p.Tyr101HisfsTer?
ENST00000611625.4:c.301_314del	ENSP00000481063.1:p.Tyr101HisfsTer?
ENST00000612417.4:c.301_314del	ENSP00000478360.1:p.Tyr101HisfsTer?
ENST00000621016.4:c.301_314del	ENSP00000480664.1:p.Tyr101HisfsTer?
NM_004360.3:c.301_314del , LRG_301t1:c.301_314del	NP_004351.1:p.Tyr101HisfsTer?
XM_011523488.1:c.-435_-422del	XP_011521790.1:n.-435_-422del
XM_011523489.1:c.-435_-422del	XP_011521791.1:n.-435_-422del
NM_001317184.1:c.301_314del	NP_001304113.1:p.Tyr101HisfsTer?
NM_001317185.1:c.-1315_-1302del	NP_001304114.1:n.-1315_-1302del
NM_001317186.1:c.-1519_-1506del	NP_001304115.1:n.-1519_-1506del
NM_004360.4:c.301_314del	NP_004351.1:p.Tyr101HisfsTer?
NM_004360.5:c.301_314del MANE Select	NP_004351.1:p.Tyr101HisfsTer?
NM_001317184.2:c.301_314del	NP_001304113.1:p.Tyr101HisfsTer?
NM_001317185.2:c.-1315_-1302del	NP_001304114.1:n.-1315_-1302del
NM_001317186.2:c.-1519_-1506del	NP_001304115.1:n.-1519_-1506del