Canonical Allele Identifier: CA396472367
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs767315263

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833393T>A , CM000678.2:g.68833393T>A GRCh38
NC_000016.9:g.68867296T>A , CM000678.1:g.68867296T>A GRCh37
NC_000016.8:g.67424797T>A NCBI36
NG_008021.1:g.101102T>A , LRG_301:g.101102T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2543T>A MANE Select ENSP00000261769.4:p.Leu848Gln
ENST00000261769.9:c.2543T>A ENSP00000261769.4:p.Leu848Gln
ENST00000422392.6:c.2360T>A ENSP00000414946.2:p.Leu787Gln
ENST00000562118.1:n.761T>A
ENST00000562836.5:n.2614T>A
ENST00000566510.5:c.*1209T>A ENSP00000458139.1:n.*1209T>A
ENST00000566612.5:c.*783T>A ENSP00000454782.1:n.*783T>A
ENST00000611625.4:c.2606T>A ENSP00000481063.1:p.Leu869Gln
ENST00000612417.4:c.1854-798T>A ENSP00000478360.1:n.1854-798T>A
ENST00000621016.4:c.1866-810T>A ENSP00000480664.1:n.1866-810T>A
NM_004360.3:c.2543T>A , LRG_301t1:c.2543T>A NP_004351.1:p.Leu848Gln
XM_011523488.1:c.1808T>A XP_011521790.1:p.Leu603Gln
XM_011523489.1:c.1808T>A XP_011521791.1:p.Leu603Gln
NM_001317184.1:c.2360T>A NP_001304113.1:p.Leu787Gln
NM_001317185.1:c.995T>A NP_001304114.1:p.Leu332Gln
NM_001317186.1:c.578T>A NP_001304115.1:p.Leu193Gln
NM_004360.4:c.2543T>A NP_004351.1:p.Leu848Gln
NM_004360.5:c.2543T>A MANE Select NP_004351.1:p.Leu848Gln
NM_001317184.2:c.2360T>A NP_001304113.1:p.Leu787Gln
NM_001317185.2:c.995T>A NP_001304114.1:p.Leu332Gln
NM_001317186.2:c.578T>A NP_001304115.1:p.Leu193Gln