Canonical Allele Identifier: CA396470823
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829670A>C , CM000678.2:g.68829670A>C GRCh38
NC_000016.9:g.68863573A>C , CM000678.1:g.68863573A>C GRCh37
NC_000016.8:g.67421074A>C NCBI36
NG_008021.1:g.97379A>C , LRG_301:g.97379A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2312A>C MANE Select ENSP00000261769.4:p.Gln771Pro
ENST00000261769.9:c.2312A>C ENSP00000261769.4:p.Gln771Pro
ENST00000422392.6:c.2129A>C ENSP00000414946.2:p.Gln710Pro
ENST00000562118.1:n.530A>C
ENST00000562836.5:n.2383A>C
ENST00000566510.5:c.*978A>C ENSP00000458139.1:n.*978A>C
ENST00000566612.5:c.*552A>C ENSP00000454782.1:n.*552A>C
ENST00000611625.4:c.2375A>C ENSP00000481063.1:p.Gln792Pro
ENST00000612417.4:c.1853+3116A>C ENSP00000478360.1:n.1853+3116A>C
ENST00000621016.4:c.1866-4533A>C ENSP00000480664.1:n.1866-4533A>C
NM_004360.3:c.2312A>C , LRG_301t1:c.2312A>C NP_004351.1:p.Gln771Pro
XM_011523488.1:c.1577A>C XP_011521790.1:p.Gln526Pro
XM_011523489.1:c.1577A>C XP_011521791.1:p.Gln526Pro
NM_001317184.1:c.2129A>C NP_001304113.1:p.Gln710Pro
NM_001317185.1:c.764A>C NP_001304114.1:p.Gln255Pro
NM_001317186.1:c.347A>C NP_001304115.1:p.Gln116Pro
NM_004360.4:c.2312A>C NP_004351.1:p.Gln771Pro
NM_004360.5:c.2312A>C MANE Select NP_004351.1:p.Gln771Pro
NM_001317184.2:c.2129A>C NP_001304113.1:p.Gln710Pro
NM_001317185.2:c.764A>C NP_001304114.1:p.Gln255Pro
NM_001317186.2:c.347A>C NP_001304115.1:p.Gln116Pro