Canonical Allele Identifier: CA396471074
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1567516121

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829724C>A , CM000678.2:g.68829724C>A GRCh38
NC_000016.9:g.68863627C>A , CM000678.1:g.68863627C>A GRCh37
NC_000016.8:g.67421128C>A NCBI36
NG_008021.1:g.97433C>A , LRG_301:g.97433C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2366C>A MANE Select ENSP00000261769.4:p.Pro789Gln
ENST00000261769.9:c.2366C>A ENSP00000261769.4:p.Pro789Gln
ENST00000422392.6:c.2183C>A ENSP00000414946.2:p.Pro728Gln
ENST00000562118.1:n.584C>A
ENST00000562836.5:n.2437C>A
ENST00000566510.5:c.*1032C>A ENSP00000458139.1:n.*1032C>A
ENST00000566612.5:c.*606C>A ENSP00000454782.1:n.*606C>A
ENST00000611625.4:c.2429C>A ENSP00000481063.1:p.Pro810Gln
ENST00000612417.4:c.1853+3170C>A ENSP00000478360.1:n.1853+3170C>A
ENST00000621016.4:c.1866-4479C>A ENSP00000480664.1:n.1866-4479C>A
NM_004360.3:c.2366C>A , LRG_301t1:c.2366C>A NP_004351.1:p.Pro789Gln
XM_011523488.1:c.1631C>A XP_011521790.1:p.Pro544Gln
XM_011523489.1:c.1631C>A XP_011521791.1:p.Pro544Gln
NM_001317184.1:c.2183C>A NP_001304113.1:p.Pro728Gln
NM_001317185.1:c.818C>A NP_001304114.1:p.Pro273Gln
NM_001317186.1:c.401C>A NP_001304115.1:p.Pro134Gln
NM_004360.4:c.2366C>A NP_004351.1:p.Pro789Gln
NM_004360.5:c.2366C>A MANE Select NP_004351.1:p.Pro789Gln
NM_001317184.2:c.2183C>A NP_001304113.1:p.Pro728Gln
NM_001317185.2:c.818C>A NP_001304114.1:p.Pro273Gln
NM_001317186.2:c.401C>A NP_001304115.1:p.Pro134Gln