Canonical Allele Identifier: CA2229980391
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68822047T= , CM000678.2:g.68822047T= GRCh38
NC_000016.9:g.68855950T= , CM000678.1:g.68855950T= GRCh37
NC_000016.8:g.67413451T= NCBI36
NG_008021.1:g.89756T= , LRG_301:g.89756T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1758T= MANE Select ENSP00000261769.4:p.Ser586=
ENST00000261769.9:c.1758T= ENSP00000261769.4:p.Ser586=
ENST00000422392.6:c.1575T= ENSP00000414946.2:p.Ser525=
ENST00000562836.5:n.1829T=
ENST00000566510.5:c.*424T= ENSP00000458139.1:n.*424T=
ENST00000566612.5:c.1612T= ENSP00000454782.1:p.Ter538=
ENST00000611625.4:c.1821T= ENSP00000481063.1:p.Ser607=
ENST00000612417.4:c.1758T= ENSP00000478360.1:p.Ser586=
ENST00000621016.4:c.1758T= ENSP00000480664.1:p.Ser586=
NM_004360.3:c.1758T= , LRG_301t1:c.1758T= NP_004351.1:p.Ser586=
XM_011523488.1:c.1023T= XP_011521790.1:p.Ser341=
XM_011523489.1:c.1023T= XP_011521791.1:p.Ser341=
NM_001317184.1:c.1575T= NP_001304113.1:p.Ser525=
NM_001317185.1:c.210T= NP_001304114.1:p.Ser70=
NM_001317186.1:c.-208T= NP_001304115.1:n.-208T=
NM_004360.4:c.1758T= NP_004351.1:p.Ser586=
NM_004360.5:c.1758T= MANE Select NP_004351.1:p.Ser586=
NM_001317184.2:c.1575T= NP_001304113.1:p.Ser525=
NM_001317185.2:c.210T= NP_001304114.1:p.Ser70=
NM_001317186.2:c.-208T= NP_001304115.1:n.-208T=