Canonical Allele Identifier: CA2229956990
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1960500799

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68801619_68801621del , CM000678.2:g.68801619_68801621del GRCh38
NC_000016.9:g.68835522_68835524del , CM000678.1:g.68835522_68835524del GRCh37
NC_000016.8:g.67393023_67393025del NCBI36
NG_008021.1:g.69328_69330del , LRG_301:g.69328_69330del

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.164-51_164-49del MANE Select ENSP00000261769.4:n.164-51_164-49del
ENST00000261769.9:c.164-51_164-49del ENSP00000261769.4:n.164-51_164-49del
ENST00000422392.6:c.164-51_164-49del ENSP00000414946.2:n.164-51_164-49del
ENST00000562836.5:n.235-51_235-49del
ENST00000564676.5:n.446-51_446-49del
ENST00000564745.1:n.159-51_159-49del
ENST00000566510.5:c.164-51_164-49del ENSP00000458139.1:n.164-51_164-49del
ENST00000566612.5:c.164-51_164-49del ENSP00000454782.1:n.164-51_164-49del
ENST00000611625.4:c.164-51_164-49del ENSP00000481063.1:n.164-51_164-49del
ENST00000612417.4:c.164-51_164-49del ENSP00000478360.1:n.164-51_164-49del
ENST00000621016.4:c.164-51_164-49del ENSP00000480664.1:n.164-51_164-49del
NM_004360.3:c.164-51_164-49del , LRG_301t1:c.164-51_164-49del NP_004351.1:n.164-51_164-49del
XM_011523488.1:c.-572-51_-572-49del XP_011521790.1:n.-572-51_-572-49del
XM_011523489.1:c.-572-51_-572-49del XP_011521791.1:n.-572-51_-572-49del
NM_001317184.1:c.164-51_164-49del NP_001304113.1:n.164-51_164-49del
NM_001317185.1:c.-1452-51_-1452-49del NP_001304114.1:n.-1452-51_-1452-49del
NM_001317186.1:c.-1656-51_-1656-49del NP_001304115.1:n.-1656-51_-1656-49del
NM_004360.4:c.164-51_164-49del NP_004351.1:n.164-51_164-49del
NM_004360.5:c.164-51_164-49del MANE Select NP_004351.1:n.164-51_164-49del
NM_001317184.2:c.164-51_164-49del NP_001304113.1:n.164-51_164-49del
NM_001317185.2:c.-1452-51_-1452-49del NP_001304114.1:n.-1452-51_-1452-49del
NM_001317186.2:c.-1656-51_-1656-49del NP_001304115.1:n.-1656-51_-1656-49del