Canonical Allele Identifier: CA157969
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 12246
dbSNP Id: rs35572355

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833344G>A , CM000678.2:g.68833344G>A GRCh38
NC_000016.9:g.68867247G>A , CM000678.1:g.68867247G>A GRCh37
NC_000016.8:g.67424748G>A NCBI36
NG_008021.1:g.101053G>A , LRG_301:g.101053G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2494G>A MANE Select ENSP00000261769.4:p.Val832Met
ENST00000261769.9:c.2494G>A ENSP00000261769.4:p.Val832Met
ENST00000422392.6:c.2311G>A ENSP00000414946.2:p.Val771Met
ENST00000562118.1:n.712G>A
ENST00000562836.5:n.2565G>A
ENST00000566510.5:c.*1160G>A ENSP00000458139.1:n.*1160G>A
ENST00000566612.5:c.*734G>A ENSP00000454782.1:n.*734G>A
ENST00000611625.4:c.2557G>A ENSP00000481063.1:p.Val853Met
ENST00000612417.4:c.1854-847G>A ENSP00000478360.1:n.1854-847G>A
ENST00000621016.4:c.1866-859G>A ENSP00000480664.1:n.1866-859G>A
NM_004360.3:c.2494G>A , LRG_301t1:c.2494G>A NP_004351.1:p.Val832Met
XM_011523488.1:c.1759G>A XP_011521790.1:p.Val587Met
XM_011523489.1:c.1759G>A XP_011521791.1:p.Val587Met
NM_001317184.1:c.2311G>A NP_001304113.1:p.Val771Met
NM_001317185.1:c.946G>A NP_001304114.1:p.Val316Met
NM_001317186.1:c.529G>A NP_001304115.1:p.Val177Met
NM_004360.4:c.2494G>A NP_004351.1:p.Val832Met
NM_004360.5:c.2494G>A MANE Select NP_004351.1:p.Val832Met
NM_001317184.2:c.2311G>A NP_001304113.1:p.Val771Met
NM_001317185.2:c.946G>A NP_001304114.1:p.Val316Met
NM_001317186.2:c.529G>A NP_001304115.1:p.Val177Met