Canonical Allele Identifier: CA2229967244
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810324T= , CM000678.2:g.68810324T= GRCh38
NC_000016.9:g.68844227T= , CM000678.1:g.68844227T= GRCh37
NC_000016.8:g.67401728T= NCBI36
NG_008021.1:g.78033T= , LRG_301:g.78033T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.815T= MANE Select ENSP00000261769.4:p.Met272=
ENST00000261769.9:c.815T= ENSP00000261769.4:p.Met272=
ENST00000422392.6:c.815T= ENSP00000414946.2:p.Met272=
ENST00000561751.1:c.455-1360T=
ENST00000562836.5:n.886T=
ENST00000566510.5:c.659T= ENSP00000458139.1:p.Met220=
ENST00000566612.5:c.815T= ENSP00000454782.1:p.Met272=
ENST00000611625.4:c.815T= ENSP00000481063.1:p.Met272=
ENST00000612417.4:c.815T= ENSP00000478360.1:p.Met272=
ENST00000621016.4:c.815T= ENSP00000480664.1:p.Met272=
NM_004360.3:c.815T= , LRG_301t1:c.815T= NP_004351.1:p.Met272=
XM_011523488.1:c.80T= XP_011521790.1:p.Met27=
XM_011523489.1:c.80T= XP_011521791.1:p.Met27=
NM_001317184.1:c.815T= NP_001304113.1:p.Met272=
NM_001317185.1:c.-801T= NP_001304114.1:n.-801T=
NM_001317186.1:c.-1005T= NP_001304115.1:n.-1005T=
NM_004360.4:c.815T= NP_004351.1:p.Met272=
NM_004360.5:c.815T= MANE Select NP_004351.1:p.Met272=
NM_001317184.2:c.815T= NP_001304113.1:p.Met272=
NM_001317185.2:c.-801T= NP_001304114.1:n.-801T=
NM_001317186.2:c.-1005T= NP_001304115.1:n.-1005T=