Canonical Allele Identifier: CA2229957927
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68801817A= , CM000678.2:g.68801817A= GRCh38
NC_000016.9:g.68835720A= , CM000678.1:g.68835720A= GRCh37
NC_000016.8:g.67393221A= NCBI36
NG_008021.1:g.69526A= , LRG_301:g.69526A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.311A= MANE Select ENSP00000261769.4:p.Asp104=
ENST00000261769.9:c.311A= ENSP00000261769.4:p.Asp104=
ENST00000422392.6:c.311A= ENSP00000414946.2:p.Asp104=
ENST00000561751.1:c.78A=
ENST00000562836.5:n.382A=
ENST00000564676.5:n.593A=
ENST00000564745.1:n.306A=
ENST00000566510.5:c.311A= ENSP00000458139.1:p.Asp104=
ENST00000566612.5:c.311A= ENSP00000454782.1:p.Asp104=
ENST00000611625.4:c.311A= ENSP00000481063.1:p.Asp104=
ENST00000612417.4:c.311A= ENSP00000478360.1:p.Asp104=
ENST00000621016.4:c.311A= ENSP00000480664.1:p.Asp104=
NM_004360.3:c.311A= , LRG_301t1:c.311A= NP_004351.1:p.Asp104=
XM_011523488.1:c.-425A= XP_011521790.1:n.-425A=
XM_011523489.1:c.-425A= XP_011521791.1:n.-425A=
NM_001317184.1:c.311A= NP_001304113.1:p.Asp104=
NM_001317185.1:c.-1305A= NP_001304114.1:n.-1305A=
NM_001317186.1:c.-1509A= NP_001304115.1:n.-1509A=
NM_004360.4:c.311A= NP_004351.1:p.Asp104=
NM_004360.5:c.311A= MANE Select NP_004351.1:p.Asp104=
NM_001317184.2:c.311A= NP_001304113.1:p.Asp104=
NM_001317185.2:c.-1305A= NP_001304114.1:n.-1305A=
NM_001317186.2:c.-1509A= NP_001304115.1:n.-1509A=