Canonical Allele Identifier: CA496392208
Gene: CDH1 HGNC NCBI

Linked Data

COSMIC: COSM435586
MyVariant Identifiers: chr16:g.68842414del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68808512del , CM000678.2:g.68808512del GRCh38
NC_000016.9:g.68842415del , CM000678.1:g.68842415del GRCh37
NC_000016.8:g.67399916del NCBI36
NG_008021.1:g.76221del , LRG_301:g.76221del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.476del MANE Select ENSP00000261769.4:p.Pro159LeufsTer?
ENST00000261769.9:c.476del ENSP00000261769.4:p.Pro159LeufsTer?
ENST00000422392.6:c.476del ENSP00000414946.2:p.Pro159LeufsTer?
ENST00000561751.1:c.243del
ENST00000562836.5:n.547del
ENST00000564676.5:n.758del
ENST00000564745.1:n.471del
ENST00000566510.5:c.476del ENSP00000458139.1:p.Pro159LeufsTer?
ENST00000566612.5:c.476del ENSP00000454782.1:p.Pro159LeufsTer?
ENST00000611625.4:c.476del ENSP00000481063.1:p.Pro159LeufsTer?
ENST00000612417.4:c.476del ENSP00000478360.1:p.Pro159LeufsTer?
ENST00000621016.4:c.476del ENSP00000480664.1:p.Pro159LeufsTer?
NM_004360.3:c.476del , LRG_301t1:c.476del NP_004351.1:p.Pro159LeufsTer?
XM_011523488.1:c.-260del XP_011521790.1:n.-260del
XM_011523489.1:c.-260del XP_011521791.1:n.-260del
NM_001317184.1:c.476del NP_001304113.1:p.Pro159LeufsTer?
NM_001317185.1:c.-1140del NP_001304114.1:n.-1140del
NM_001317186.1:c.-1344del NP_001304115.1:n.-1344del
NM_004360.4:c.476del NP_004351.1:p.Pro159LeufsTer?
NM_004360.5:c.476del MANE Select NP_004351.1:p.Pro159LeufsTer?
NM_001317184.2:c.476del NP_001304113.1:p.Pro159LeufsTer?
NM_001317185.2:c.-1140del NP_001304114.1:n.-1140del
NM_001317186.2:c.-1344del NP_001304115.1:n.-1344del