Canonical Allele Identifier: CA723143315
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1462515714

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829511_68829512del , CM000678.2:g.68829511_68829512del GRCh38
NC_000016.9:g.68863414_68863415del , CM000678.1:g.68863414_68863415del GRCh37
NC_000016.8:g.67420915_67420916del NCBI36
NG_008021.1:g.97220_97221del , LRG_301:g.97220_97221del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2296-143_2296-142del MANE Select ENSP00000261769.4:n.2296-143_2296-142del
ENST00000261769.9:c.2296-143_2296-142del ENSP00000261769.4:n.2296-143_2296-142del
ENST00000422392.6:c.2113-143_2113-142del ENSP00000414946.2:n.2113-143_2113-142del
ENST00000562118.1:n.514-143_514-142del
ENST00000562836.5:n.2367-143_2367-142del
ENST00000566510.5:c.*962-143_*962-142del ENSP00000458139.1:n.*962-143_*962-142del
ENST00000566612.5:c.*536-143_*536-142del ENSP00000454782.1:n.*536-143_*536-142del
ENST00000611625.4:c.2359-143_2359-142del ENSP00000481063.1:n.2359-143_2359-142del
ENST00000612417.4:c.1853+2957_1853+2958del ENSP00000478360.1:n.1853+2957_1853+2958del
ENST00000621016.4:c.1866-4692_1866-4691del ENSP00000480664.1:n.1866-4692_1866-4691del
NM_004360.3:c.2296-143_2296-142del , LRG_301t1:c.2296-143_2296-142del NP_004351.1:n.2296-143_2296-142del
XM_011523488.1:c.1561-143_1561-142del XP_011521790.1:n.1561-143_1561-142del
XM_011523489.1:c.1561-143_1561-142del XP_011521791.1:n.1561-143_1561-142del
NM_001317184.1:c.2113-143_2113-142del NP_001304113.1:n.2113-143_2113-142del
NM_001317185.1:c.748-143_748-142del NP_001304114.1:n.748-143_748-142del
NM_001317186.1:c.331-143_331-142del NP_001304115.1:n.331-143_331-142del
NM_004360.4:c.2296-143_2296-142del NP_004351.1:n.2296-143_2296-142del
NM_004360.5:c.2296-143_2296-142del MANE Select NP_004351.1:n.2296-143_2296-142del
NM_001317184.2:c.2113-143_2113-142del NP_001304113.1:n.2113-143_2113-142del
NM_001317185.2:c.748-143_748-142del NP_001304114.1:n.748-143_748-142del
NM_001317186.2:c.331-143_331-142del NP_001304115.1:n.331-143_331-142del