Canonical Allele Identifier: CA645596590
Gene: CDH1 HGNC NCBI

Linked Data

COSMIC: COSM28934

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68801747_68801750dup , CM000678.2:g.68801747_68801750dup GRCh38
NC_000016.9:g.68835650_68835653dup , CM000678.1:g.68835650_68835653dup GRCh37
NC_000016.8:g.67393151_67393154dup NCBI36
NG_008021.1:g.69456_69459dup , LRG_301:g.69456_69459dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.241_244dup MANE Select ENSP00000261769.4:p.Val82GlyfsTer13
ENST00000261769.9:c.241_244dup ENSP00000261769.4:p.Val82GlyfsTer13
ENST00000422392.6:c.241_244dup ENSP00000414946.2:p.Val82GlyfsTer13
ENST00000561751.1:c.8_11dup
ENST00000562836.5:n.312_315dup
ENST00000564676.5:n.523_526dup
ENST00000564745.1:n.236_239dup
ENST00000566510.5:c.241_244dup ENSP00000458139.1:p.Val82GlyfsTer13
ENST00000566612.5:c.241_244dup ENSP00000454782.1:p.Val82GlyfsTer13
ENST00000611625.4:c.241_244dup ENSP00000481063.1:p.Val82GlyfsTer13
ENST00000612417.4:c.241_244dup ENSP00000478360.1:p.Val82GlyfsTer13
ENST00000621016.4:c.241_244dup ENSP00000480664.1:p.Val82GlyfsTer13
NM_004360.3:c.241_244dup , LRG_301t1:c.241_244dup NP_004351.1:p.Val82GlyfsTer13
XM_011523488.1:c.-495_-492dup XP_011521790.1:n.-495_-492dup
XM_011523489.1:c.-495_-492dup XP_011521791.1:n.-495_-492dup
NM_001317184.1:c.241_244dup NP_001304113.1:p.Val82GlyfsTer13
NM_001317185.1:c.-1375_-1372dup NP_001304114.1:n.-1375_-1372dup
NM_001317186.1:c.-1579_-1576dup NP_001304115.1:n.-1579_-1576dup
NM_004360.4:c.241_244dup NP_004351.1:p.Val82GlyfsTer13
NM_004360.5:c.241_244dup MANE Select NP_004351.1:p.Val82GlyfsTer13
NM_001317184.2:c.241_244dup NP_001304113.1:p.Val82GlyfsTer13
NM_001317185.2:c.-1375_-1372dup NP_001304114.1:n.-1375_-1372dup
NM_001317186.2:c.-1579_-1576dup NP_001304115.1:n.-1579_-1576dup