Canonical Allele Identifier: CA496392708
Gene: CDH1 HGNC NCBI

Linked Data

COSMIC: COSM19535
MyVariant Identifiers: chr16:g.68856036del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68822134del , CM000678.2:g.68822134del GRCh38
NC_000016.9:g.68856037del , CM000678.1:g.68856037del GRCh37
NC_000016.8:g.67413538del NCBI36
NG_008021.1:g.89843del , LRG_301:g.89843del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1845del MANE Select ENSP00000261769.4:p.Ile615MetfsTer16
ENST00000261769.9:c.1845del ENSP00000261769.4:p.Ile615MetfsTer16
ENST00000422392.6:c.1662del ENSP00000414946.2:p.Ile554MetfsTer16
ENST00000562836.5:n.1916del
ENST00000566510.5:c.*511del ENSP00000458139.1:n.*511del
ENST00000566612.5:c.*85del ENSP00000454782.1:n.*85del
ENST00000611625.4:c.1908del ENSP00000481063.1:p.Ile636MetfsTer16
ENST00000612417.4:c.1830+15del ENSP00000478360.1:n.1830+15del
ENST00000621016.4:c.1845del ENSP00000480664.1:p.Ile615MetfsTer19
NM_004360.3:c.1845del , LRG_301t1:c.1845del NP_004351.1:p.Ile615MetfsTer16
XM_011523488.1:c.1110del XP_011521790.1:p.Ile370MetfsTer16
XM_011523489.1:c.1110del XP_011521791.1:p.Ile370MetfsTer16
NM_001317184.1:c.1662del NP_001304113.1:p.Ile554MetfsTer16
NM_001317185.1:c.297del NP_001304114.1:p.Ile99MetfsTer16
NM_001317186.1:c.-121del NP_001304115.1:n.-121del
NM_004360.4:c.1845del NP_004351.1:p.Ile615MetfsTer16
NM_004360.5:c.1845del MANE Select NP_004351.1:p.Ile615MetfsTer16
NM_001317184.2:c.1662del NP_001304113.1:p.Ile554MetfsTer16
NM_001317185.2:c.297del NP_001304114.1:p.Ile99MetfsTer16
NM_001317186.2:c.-121del NP_001304115.1:n.-121del