Canonical Allele Identifier: CA496393066
Gene: CDH1 HGNC NCBI

Linked Data

COSMIC: COSM19538
MyVariant Identifiers: chr16:g.68857336del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68823433del , CM000678.2:g.68823433del GRCh38
NC_000016.9:g.68857336del , CM000678.1:g.68857336del GRCh37
NC_000016.8:g.67414837del NCBI36
NG_008021.1:g.91142del , LRG_301:g.91142del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1971del MANE Select ENSP00000261769.4:p.Leu658Ter
ENST00000261769.9:c.1971del ENSP00000261769.4:p.Leu658Ter
ENST00000422392.6:c.1788del ENSP00000414946.2:p.Leu597Ter
ENST00000562118.1:n.189del
ENST00000562836.5:n.2042del
ENST00000566510.5:c.*637del ENSP00000458139.1:n.*637del
ENST00000566612.5:c.*211del ENSP00000454782.1:n.*211del
ENST00000611625.4:c.2034del ENSP00000481063.1:p.Leu679Ter
ENST00000612417.4:c.1830+1314del ENSP00000478360.1:n.1830+1314del
ENST00000621016.4:c.1865+1279del ENSP00000480664.1:n.1865+1279del
NM_004360.3:c.1971del , LRG_301t1:c.1971del NP_004351.1:p.Leu658Ter
XM_011523488.1:c.1236del XP_011521790.1:p.Leu413Ter
XM_011523489.1:c.1236del XP_011521791.1:p.Leu413Ter
NM_001317184.1:c.1788del NP_001304113.1:p.Leu597Ter
NM_001317185.1:c.423del NP_001304114.1:p.Leu142Ter
NM_001317186.1:c.6del NP_001304115.1:p.Leu3Ter
NM_004360.4:c.1971del NP_004351.1:p.Leu658Ter
NM_004360.5:c.1971del MANE Select NP_004351.1:p.Leu658Ter
NM_001317184.2:c.1788del NP_001304113.1:p.Leu597Ter
NM_001317185.2:c.423del NP_001304114.1:p.Leu142Ter
NM_001317186.2:c.6del NP_001304115.1:p.Leu3Ter