Canonical Allele Identifier: CA2732920486
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2152142323

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829714_68829723del , CM000678.2:g.68829714_68829723del GRCh38
NC_000016.9:g.68863617_68863626del , CM000678.1:g.68863617_68863626del GRCh37
NC_000016.8:g.67421118_67421127del NCBI36
NG_008021.1:g.97423_97432del , LRG_301:g.97423_97432del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2356_2365del MANE Select ENSP00000261769.4:p.Asp786GlnfsTer4
ENST00000261769.9:c.2356_2365del ENSP00000261769.4:p.Asp786GlnfsTer4
ENST00000422392.6:c.2173_2182del ENSP00000414946.2:p.Asp725GlnfsTer4
ENST00000562118.1:n.574_583del
ENST00000562836.5:n.2427_2436del
ENST00000566510.5:c.*1022_*1031del ENSP00000458139.1:n.*1022_*1031del
ENST00000566612.5:c.*596_*605del ENSP00000454782.1:n.*596_*605del
ENST00000611625.4:c.2419_2428del ENSP00000481063.1:p.Asp807GlnfsTer4
ENST00000612417.4:c.1853+3160_1853+3169del ENSP00000478360.1:n.1853+3160_1853+3169del
ENST00000621016.4:c.1866-4489_1866-4480del ENSP00000480664.1:n.1866-4489_1866-4480del
NM_004360.3:c.2356_2365del , LRG_301t1:c.2356_2365del NP_004351.1:p.Asp786GlnfsTer4
XM_011523488.1:c.1621_1630del XP_011521790.1:p.Asp541GlnfsTer4
XM_011523489.1:c.1621_1630del XP_011521791.1:p.Asp541GlnfsTer4
NM_001317184.1:c.2173_2182del NP_001304113.1:p.Asp725GlnfsTer4
NM_001317185.1:c.808_817del NP_001304114.1:p.Asp270GlnfsTer4
NM_001317186.1:c.391_400del NP_001304115.1:p.Asp131GlnfsTer4
NM_004360.4:c.2356_2365del NP_004351.1:p.Asp786GlnfsTer4
NM_004360.5:c.2356_2365del MANE Select NP_004351.1:p.Asp786GlnfsTer4
NM_001317184.2:c.2173_2182del NP_001304113.1:p.Asp725GlnfsTer4
NM_001317185.2:c.808_817del NP_001304114.1:p.Asp270GlnfsTer4
NM_001317186.2:c.391_400del NP_001304115.1:p.Asp131GlnfsTer4