Canonical Allele Identifier: CA2732921370
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs2152142509

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829816_68829824del , CM000678.2:g.68829816_68829824del GRCh38
NC_000016.9:g.68863719_68863727del , CM000678.1:g.68863719_68863727del GRCh37
NC_000016.8:g.67421220_67421228del NCBI36
NG_008021.1:g.97525_97533del , LRG_301:g.97525_97533del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2439+19_2439+27del MANE Select ENSP00000261769.4:n.2439+19_2439+27del
ENST00000261769.9:c.2439+19_2439+27del ENSP00000261769.4:n.2439+19_2439+27del
ENST00000422392.6:c.2256+19_2256+27del ENSP00000414946.2:n.2256+19_2256+27del
ENST00000562118.1:n.657+19_657+27del
ENST00000562836.5:n.2510+19_2510+27del
ENST00000566510.5:c.*1105+19_*1105+27del ENSP00000458139.1:n.*1105+19_*1105+27del
ENST00000566612.5:c.*679+19_*679+27del ENSP00000454782.1:n.*679+19_*679+27del
ENST00000611625.4:c.2502+19_2502+27del ENSP00000481063.1:n.2502+19_2502+27del
ENST00000612417.4:c.1853+3262_1853+3270del ENSP00000478360.1:n.1853+3262_1853+3270del
ENST00000621016.4:c.1866-4387_1866-4379del ENSP00000480664.1:n.1866-4387_1866-4379del
NM_004360.3:c.2439+19_2439+27del , LRG_301t1:c.2439+19_2439+27del NP_004351.1:n.2439+19_2439+27del
XM_011523488.1:c.1704+19_1704+27del XP_011521790.1:n.1704+19_1704+27del
XM_011523489.1:c.1704+19_1704+27del XP_011521791.1:n.1704+19_1704+27del
NM_001317184.1:c.2256+19_2256+27del NP_001304113.1:n.2256+19_2256+27del
NM_001317185.1:c.891+19_891+27del NP_001304114.1:n.891+19_891+27del
NM_001317186.1:c.474+19_474+27del NP_001304115.1:n.474+19_474+27del
NM_004360.4:c.2439+19_2439+27del NP_004351.1:n.2439+19_2439+27del
NM_004360.5:c.2439+19_2439+27del MANE Select NP_004351.1:n.2439+19_2439+27del
NM_001317184.2:c.2256+19_2256+27del NP_001304113.1:n.2256+19_2256+27del
NM_001317185.2:c.891+19_891+27del NP_001304114.1:n.891+19_891+27del
NM_001317186.2:c.474+19_474+27del NP_001304115.1:n.474+19_474+27del