Canonical Allele Identifier: CA2229980978
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68822196C= , CM000678.2:g.68822196C= GRCh38
NC_000016.9:g.68856099C= , CM000678.1:g.68856099C= GRCh37
NC_000016.8:g.67413600C= NCBI36
NG_008021.1:g.89905C= , LRG_301:g.89905C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1907C= MANE Select ENSP00000261769.4:p.Ala636=
ENST00000261769.9:c.1907C= ENSP00000261769.4:p.Ala636=
ENST00000422392.6:c.1724C= ENSP00000414946.2:p.Ala575=
ENST00000562836.5:n.1978C=
ENST00000566510.5:c.*573C= ENSP00000458139.1:n.*573C=
ENST00000566612.5:c.*147C= ENSP00000454782.1:n.*147C=
ENST00000611625.4:c.1970C= ENSP00000481063.1:p.Ala657=
ENST00000612417.4:c.1830+77C= ENSP00000478360.1:n.1830+77C=
ENST00000621016.4:c.1865+42C= ENSP00000480664.1:n.1865+42C=
NM_004360.3:c.1907C= , LRG_301t1:c.1907C= NP_004351.1:p.Ala636=
XM_011523488.1:c.1172C= XP_011521790.1:p.Ala391=
XM_011523489.1:c.1172C= XP_011521791.1:p.Ala391=
NM_001317184.1:c.1724C= NP_001304113.1:p.Ala575=
NM_001317185.1:c.359C= NP_001304114.1:p.Ala120=
NM_001317186.1:c.-59C= NP_001304115.1:n.-59C=
NM_004360.4:c.1907C= NP_004351.1:p.Ala636=
NM_004360.5:c.1907C= MANE Select NP_004351.1:p.Ala636=
NM_001317184.2:c.1724C= NP_001304113.1:p.Ala575=
NM_001317185.2:c.359C= NP_001304114.1:p.Ala120=
NM_001317186.2:c.-59C= NP_001304115.1:n.-59C=