Canonical Allele Identifier: CA2229978122
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833309C= , CM000678.2:g.68833309C= GRCh38
NC_000016.9:g.68867212C= , CM000678.1:g.68867212C= GRCh37
NC_000016.8:g.67424713C= NCBI36
NG_008021.1:g.101018C= , LRG_301:g.101018C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2459C= MANE Select ENSP00000261769.4:p.Thr820=
ENST00000261769.9:c.2459C= ENSP00000261769.4:p.Thr820=
ENST00000422392.6:c.2276C= ENSP00000414946.2:p.Thr759=
ENST00000562118.1:n.677C=
ENST00000562836.5:n.2530C=
ENST00000566510.5:c.*1125C= ENSP00000458139.1:n.*1125C=
ENST00000566612.5:c.*699C= ENSP00000454782.1:n.*699C=
ENST00000611625.4:c.2522C= ENSP00000481063.1:p.Thr841=
ENST00000612417.4:c.1854-882C= ENSP00000478360.1:n.1854-882C=
ENST00000621016.4:c.1866-894C= ENSP00000480664.1:n.1866-894C=
NM_004360.3:c.2459C= , LRG_301t1:c.2459C= NP_004351.1:p.Thr820=
XM_011523488.1:c.1724C= XP_011521790.1:p.Thr575=
XM_011523489.1:c.1724C= XP_011521791.1:p.Thr575=
NM_001317184.1:c.2276C= NP_001304113.1:p.Thr759=
NM_001317185.1:c.911C= NP_001304114.1:p.Thr304=
NM_001317186.1:c.494C= NP_001304115.1:p.Thr165=
NM_004360.4:c.2459C= NP_004351.1:p.Thr820=
NM_004360.5:c.2459C= MANE Select NP_004351.1:p.Thr820=
NM_001317184.2:c.2276C= NP_001304113.1:p.Thr759=
NM_001317185.2:c.911C= NP_001304114.1:p.Thr304=
NM_001317186.2:c.494C= NP_001304115.1:p.Thr165=