Canonical Allele Identifier: CA645580179
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819321_68819335del , CM000678.2:g.68819321_68819335del GRCh38
NC_000016.9:g.68853224_68853238del , CM000678.1:g.68853224_68853238del GRCh37
NC_000016.8:g.67410725_67410739del NCBI36
NG_008021.1:g.87030_87044del , LRG_301:g.87030_87044del

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.1607_1621del MANE Select ENSP00000261769.4:p.Asn536_Ala541delinsTh...
ENST00000261769.9:c.1607_1621del ENSP00000261769.4:p.Asn536_Ala541delinsTh...
ENST00000422392.6:c.1424_1438del ENSP00000414946.2:p.Asn475_Ala480delinsTh...
ENST00000562836.5:n.1678_1692del
ENST00000566510.5:c.*273_*287del ENSP00000458139.1:n.*273_*287del
ENST00000566612.5:c.1566-2680_1566-2666del ENSP00000454782.1:n.1566-2680_1566-2666de...
ENST00000611625.4:c.1670_1684del ENSP00000481063.1:p.Asn557_Ala562delinsTh...
ENST00000612417.4:c.1607_1621del ENSP00000478360.1:p.Asn536_Ala541delinsTh...
ENST00000621016.4:c.1607_1621del ENSP00000480664.1:p.Asn536_Ala541delinsTh...
NM_004360.3:c.1607_1621del , LRG_301t1:c.1607_1621del NP_004351.1:p.Asn536_Ala541delinsThr
XM_011523488.1:c.872_886del XP_011521790.1:p.Asn291_Ala296delinsThr
XM_011523489.1:c.872_886del XP_011521791.1:p.Asn291_Ala296delinsThr
NM_001317184.1:c.1424_1438del NP_001304113.1:p.Asn475_Ala480delinsThr
NM_001317185.1:c.59_73del NP_001304114.1:p.Asn20_Ala25delinsThr
NM_001317186.1:c.-254-2680_-254-2666del NP_001304115.1:n.-254-2680_-254-2666del
NM_004360.4:c.1607_1621del NP_004351.1:p.Asn536_Ala541delinsThr
NM_004360.5:c.1607_1621del MANE Select NP_004351.1:p.Asn536_Ala541delinsThr
NM_001317184.2:c.1424_1438del NP_001304113.1:p.Asn475_Ala480delinsThr
NM_001317185.2:c.59_73del NP_001304114.1:p.Asn20_Ala25delinsThr
NM_001317186.2:c.-254-2680_-254-2666del NP_001304115.1:n.-254-2680_-254-2666del