Canonical Allele Identifier: CA2229978504
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833464C= , CM000678.2:g.68833464C= GRCh38
NC_000016.9:g.68867367C= , CM000678.1:g.68867367C= GRCh37
NC_000016.8:g.67424868C= NCBI36
NG_008021.1:g.101173C= , LRG_301:g.101173C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2614C= MANE Select ENSP00000261769.4:p.Leu872=
ENST00000261769.9:c.2614C= ENSP00000261769.4:p.Leu872=
ENST00000422392.6:c.2431C= ENSP00000414946.2:p.Leu811=
ENST00000562118.1:n.832C=
ENST00000562836.5:n.2685C=
ENST00000566510.5:c.*1280C= ENSP00000458139.1:n.*1280C=
ENST00000566612.5:c.*854C= ENSP00000454782.1:n.*854C=
ENST00000611625.4:c.2677C= ENSP00000481063.1:p.Leu893=
ENST00000612417.4:c.1854-727C= ENSP00000478360.1:n.1854-727C=
ENST00000621016.4:c.1866-739C= ENSP00000480664.1:n.1866-739C=
NM_004360.3:c.2614C= , LRG_301t1:c.2614C= NP_004351.1:p.Leu872=
XM_011523488.1:c.1879C= XP_011521790.1:p.Leu627=
XM_011523489.1:c.1879C= XP_011521791.1:p.Leu627=
NM_001317184.1:c.2431C= NP_001304113.1:p.Leu811=
NM_001317185.1:c.1066C= NP_001304114.1:p.Leu356=
NM_001317186.1:c.649C= NP_001304115.1:p.Leu217=
NM_004360.4:c.2614C= NP_004351.1:p.Leu872=
NM_004360.5:c.2614C= MANE Select NP_004351.1:p.Leu872=
NM_001317184.2:c.2431C= NP_001304113.1:p.Leu811=
NM_001317185.2:c.1066C= NP_001304114.1:p.Leu356=
NM_001317186.2:c.649C= NP_001304115.1:p.Leu217=