Canonical Allele Identifier: CA2229978474
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833448C= , CM000678.2:g.68833448C= GRCh38
NC_000016.9:g.68867351C= , CM000678.1:g.68867351C= GRCh37
NC_000016.8:g.67424852C= NCBI36
NG_008021.1:g.101157C= , LRG_301:g.101157C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2598C= MANE Select ENSP00000261769.4:p.Gly866=
ENST00000261769.9:c.2598C= ENSP00000261769.4:p.Gly866=
ENST00000422392.6:c.2415C= ENSP00000414946.2:p.Gly805=
ENST00000562118.1:n.816C=
ENST00000562836.5:n.2669C=
ENST00000566510.5:c.*1264C= ENSP00000458139.1:n.*1264C=
ENST00000566612.5:c.*838C= ENSP00000454782.1:n.*838C=
ENST00000611625.4:c.2661C= ENSP00000481063.1:p.Gly887=
ENST00000612417.4:c.1854-743C= ENSP00000478360.1:n.1854-743C=
ENST00000621016.4:c.1866-755C= ENSP00000480664.1:n.1866-755C=
NM_004360.3:c.2598C= , LRG_301t1:c.2598C= NP_004351.1:p.Gly866=
XM_011523488.1:c.1863C= XP_011521790.1:p.Gly621=
XM_011523489.1:c.1863C= XP_011521791.1:p.Gly621=
NM_001317184.1:c.2415C= NP_001304113.1:p.Gly805=
NM_001317185.1:c.1050C= NP_001304114.1:p.Gly350=
NM_001317186.1:c.633C= NP_001304115.1:p.Gly211=
NM_004360.4:c.2598C= NP_004351.1:p.Gly866=
NM_004360.5:c.2598C= MANE Select NP_004351.1:p.Gly866=
NM_001317184.2:c.2415C= NP_001304113.1:p.Gly805=
NM_001317185.2:c.1050C= NP_001304114.1:p.Gly350=
NM_001317186.2:c.633C= NP_001304115.1:p.Gly211=