Canonical Allele Identifier: CA2229982711
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68823441T= , CM000678.2:g.68823441T= GRCh38
NC_000016.9:g.68857344T= , CM000678.1:g.68857344T= GRCh37
NC_000016.8:g.67414845T= NCBI36
NG_008021.1:g.91150T= , LRG_301:g.91150T=

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.1979T= MANE Select ENSP00000261769.4:p.Val660=
ENST00000261769.9:c.1979T= ENSP00000261769.4:p.Val660=
ENST00000422392.6:c.1796T= ENSP00000414946.2:p.Val599=
ENST00000562118.1:n.197T=
ENST00000562836.5:n.2050T=
ENST00000566510.5:c.*645T= ENSP00000458139.1:n.*645T=
ENST00000566612.5:c.*219T= ENSP00000454782.1:n.*219T=
ENST00000611625.4:c.2042T= ENSP00000481063.1:p.Val681=
ENST00000612417.4:c.1830+1322T= ENSP00000478360.1:n.1830+1322T=
ENST00000621016.4:c.1865+1287T= ENSP00000480664.1:n.1865+1287T=
NM_004360.3:c.1979T= , LRG_301t1:c.1979T= NP_004351.1:p.Val660=
XM_011523488.1:c.1244T= XP_011521790.1:p.Val415=
XM_011523489.1:c.1244T= XP_011521791.1:p.Val415=
NM_001317184.1:c.1796T= NP_001304113.1:p.Val599=
NM_001317185.1:c.431T= NP_001304114.1:p.Val144=
NM_001317186.1:c.14T= NP_001304115.1:p.Val5=
NM_004360.4:c.1979T= NP_004351.1:p.Val660=
NM_004360.5:c.1979T= MANE Select NP_004351.1:p.Val660=
NM_001317184.2:c.1796T= NP_001304113.1:p.Val599=
NM_001317185.2:c.431T= NP_001304114.1:p.Val144=
NM_001317186.2:c.14T= NP_001304115.1:p.Val5=