Canonical Allele Identifier: CA2229957446
Gene: CDH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68801733A= , CM000678.2:g.68801733A= GRCh38
NC_000016.9:g.68835636A= , CM000678.1:g.68835636A= GRCh37
NC_000016.8:g.67393137A= NCBI36
NG_008021.1:g.69442A= , LRG_301:g.69442A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.227A= MANE Select ENSP00000261769.4:p.Lys76=
ENST00000261769.9:c.227A= ENSP00000261769.4:p.Lys76=
ENST00000422392.6:c.227A= ENSP00000414946.2:p.Lys76=
ENST00000562836.5:n.298A=
ENST00000564676.5:n.509A=
ENST00000564745.1:n.222A=
ENST00000566510.5:c.227A= ENSP00000458139.1:p.Lys76=
ENST00000566612.5:c.227A= ENSP00000454782.1:p.Lys76=
ENST00000611625.4:c.227A= ENSP00000481063.1:p.Lys76=
ENST00000612417.4:c.227A= ENSP00000478360.1:p.Lys76=
ENST00000621016.4:c.227A= ENSP00000480664.1:p.Lys76=
NM_004360.3:c.227A= , LRG_301t1:c.227A= NP_004351.1:p.Lys76=
XM_011523488.1:c.-509A= XP_011521790.1:n.-509A=
XM_011523489.1:c.-509A= XP_011521791.1:n.-509A=
NM_001317184.1:c.227A= NP_001304113.1:p.Lys76=
NM_001317185.1:c.-1389A= NP_001304114.1:n.-1389A=
NM_001317186.1:c.-1593A= NP_001304115.1:n.-1593A=
NM_004360.4:c.227A= NP_004351.1:p.Lys76=
NM_004360.5:c.227A= MANE Select NP_004351.1:p.Lys76=
NM_001317184.2:c.227A= NP_001304113.1:p.Lys76=
NM_001317185.2:c.-1389A= NP_001304114.1:n.-1389A=
NM_001317186.2:c.-1593A= NP_001304115.1:n.-1593A=