Canonical Allele Identifier: CA2229982879
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68823471T= , CM000678.2:g.68823471T= GRCh38
NC_000016.9:g.68857374T= , CM000678.1:g.68857374T= GRCh37
NC_000016.8:g.67414875T= NCBI36
NG_008021.1:g.91180T= , LRG_301:g.91180T=

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.2009T= MANE Select ENSP00000261769.4:p.Met670=
ENST00000261769.9:c.2009T= ENSP00000261769.4:p.Met670=
ENST00000422392.6:c.1826T= ENSP00000414946.2:p.Met609=
ENST00000562118.1:n.227T=
ENST00000562836.5:n.2080T=
ENST00000566510.5:c.*675T= ENSP00000458139.1:n.*675T=
ENST00000566612.5:c.*249T= ENSP00000454782.1:n.*249T=
ENST00000611625.4:c.2072T= ENSP00000481063.1:p.Met691=
ENST00000612417.4:c.1830+1352T= ENSP00000478360.1:n.1830+1352T=
ENST00000621016.4:c.1865+1317T= ENSP00000480664.1:n.1865+1317T=
NM_004360.3:c.2009T= , LRG_301t1:c.2009T= NP_004351.1:p.Met670=
XM_011523488.1:c.1274T= XP_011521790.1:p.Met425=
XM_011523489.1:c.1274T= XP_011521791.1:p.Met425=
NM_001317184.1:c.1826T= NP_001304113.1:p.Met609=
NM_001317185.1:c.461T= NP_001304114.1:p.Met154=
NM_001317186.1:c.44T= NP_001304115.1:p.Met15=
NM_004360.4:c.2009T= NP_004351.1:p.Met670=
NM_004360.5:c.2009T= MANE Select NP_004351.1:p.Met670=
NM_001317184.2:c.1826T= NP_001304113.1:p.Met609=
NM_001317185.2:c.461T= NP_001304114.1:p.Met154=
NM_001317186.2:c.44T= NP_001304115.1:p.Met15=