Canonical Allele Identifier: CA645596592
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68801764_68801765del , CM000678.2:g.68801764_68801765del GRCh38
NC_000016.9:g.68835667_68835668del , CM000678.1:g.68835667_68835668del GRCh37
NC_000016.8:g.67393168_67393169del NCBI36
NG_008021.1:g.69473_69474del , LRG_301:g.69473_69474del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.258_259del MANE Select ENSP00000261769.4:p.Arg87AlafsTer6
ENST00000261769.9:c.258_259del ENSP00000261769.4:p.Arg87AlafsTer6
ENST00000422392.6:c.258_259del ENSP00000414946.2:p.Arg87AlafsTer6
ENST00000561751.1:c.25_26del
ENST00000562836.5:n.329_330del
ENST00000564676.5:n.540_541del
ENST00000564745.1:n.253_254del
ENST00000566510.5:c.258_259del ENSP00000458139.1:p.Arg87AlafsTer6
ENST00000566612.5:c.258_259del ENSP00000454782.1:p.Arg87AlafsTer6
ENST00000611625.4:c.258_259del ENSP00000481063.1:p.Arg87AlafsTer6
ENST00000612417.4:c.258_259del ENSP00000478360.1:p.Arg87AlafsTer6
ENST00000621016.4:c.258_259del ENSP00000480664.1:p.Arg87AlafsTer6
NM_004360.3:c.258_259del , LRG_301t1:c.258_259del NP_004351.1:p.Arg87AlafsTer6
XM_011523488.1:c.-478_-477del XP_011521790.1:n.-478_-477del
XM_011523489.1:c.-478_-477del XP_011521791.1:n.-478_-477del
NM_001317184.1:c.258_259del NP_001304113.1:p.Arg87AlafsTer6
NM_001317185.1:c.-1358_-1357del NP_001304114.1:n.-1358_-1357del
NM_001317186.1:c.-1562_-1561del NP_001304115.1:n.-1562_-1561del
NM_004360.4:c.258_259del NP_004351.1:p.Arg87AlafsTer6
NM_004360.5:c.258_259del MANE Select NP_004351.1:p.Arg87AlafsTer6
NM_001317184.2:c.258_259del NP_001304113.1:p.Arg87AlafsTer6
NM_001317185.2:c.-1358_-1357del NP_001304114.1:n.-1358_-1357del
NM_001317186.2:c.-1562_-1561del NP_001304115.1:n.-1562_-1561del