Canonical Allele Identifier: CA2229957213
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68801689C= , CM000678.2:g.68801689C= GRCh38
NC_000016.9:g.68835592C= , CM000678.1:g.68835592C= GRCh37
NC_000016.8:g.67393093C= NCBI36
NG_008021.1:g.69398C= , LRG_301:g.69398C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.183C= MANE Select ENSP00000261769.4:p.Thr61=
ENST00000261769.9:c.183C= ENSP00000261769.4:p.Thr61=
ENST00000422392.6:c.183C= ENSP00000414946.2:p.Thr61=
ENST00000562836.5:n.254C=
ENST00000564676.5:n.465C=
ENST00000564745.1:n.178C=
ENST00000566510.5:c.183C= ENSP00000458139.1:p.Thr61=
ENST00000566612.5:c.183C= ENSP00000454782.1:p.Thr61=
ENST00000611625.4:c.183C= ENSP00000481063.1:p.Thr61=
ENST00000612417.4:c.183C= ENSP00000478360.1:p.Thr61=
ENST00000621016.4:c.183C= ENSP00000480664.1:p.Thr61=
NM_004360.3:c.183C= , LRG_301t1:c.183C= NP_004351.1:p.Thr61=
XM_011523488.1:c.-553C= XP_011521790.1:n.-553C=
XM_011523489.1:c.-553C= XP_011521791.1:n.-553C=
NM_001317184.1:c.183C= NP_001304113.1:p.Thr61=
NM_001317185.1:c.-1433C= NP_001304114.1:n.-1433C=
NM_001317186.1:c.-1637C= NP_001304115.1:n.-1637C=
NM_004360.4:c.183C= NP_004351.1:p.Thr61=
NM_004360.5:c.183C= MANE Select NP_004351.1:p.Thr61=
NM_001317184.2:c.183C= NP_001304113.1:p.Thr61=
NM_001317185.2:c.-1433C= NP_001304114.1:n.-1433C=
NM_001317186.2:c.-1637C= NP_001304115.1:n.-1637C=