Canonical Allele Identifier: CA978522241
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1961064358

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819028_68819029del , CM000678.2:g.68819028_68819029del GRCh38
NC_000016.9:g.68852931_68852932del , CM000678.1:g.68852931_68852932del GRCh37
NC_000016.8:g.67410432_67410433del NCBI36
NG_008021.1:g.86737_86738del , LRG_301:g.86737_86738del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1566-252_1566-251del MANE Select ENSP00000261769.4:n.1566-252_1566-251del
ENST00000261769.9:c.1566-252_1566-251del ENSP00000261769.4:n.1566-252_1566-251del
ENST00000422392.6:c.1383-252_1383-251del ENSP00000414946.2:n.1383-252_1383-251del
ENST00000562836.5:n.1637-252_1637-251del
ENST00000566510.5:c.*232-252_*232-251del ENSP00000458139.1:n.*232-252_*232-251del
ENST00000566612.5:c.1566-2973_1566-2972del ENSP00000454782.1:n.1566-2973_1566-2972del
ENST00000611625.4:c.1629-252_1629-251del ENSP00000481063.1:n.1629-252_1629-251del
ENST00000612417.4:c.1566-252_1566-251del ENSP00000478360.1:n.1566-252_1566-251del
ENST00000621016.4:c.1566-252_1566-251del ENSP00000480664.1:n.1566-252_1566-251del
NM_004360.3:c.1566-252_1566-251del , LRG_301t1:c.1566-252_1566-251del NP_004351.1:n.1566-252_1566-251del
XM_011523488.1:c.831-252_831-251del XP_011521790.1:n.831-252_831-251del
XM_011523489.1:c.831-252_831-251del XP_011521791.1:n.831-252_831-251del
NM_001317184.1:c.1383-252_1383-251del NP_001304113.1:n.1383-252_1383-251del
NM_001317185.1:c.18-252_18-251del NP_001304114.1:n.18-252_18-251del
NM_001317186.1:c.-254-2973_-254-2972del NP_001304115.1:n.-254-2973_-254-2972del
NM_004360.4:c.1566-252_1566-251del NP_004351.1:n.1566-252_1566-251del
NM_004360.5:c.1566-252_1566-251del MANE Select NP_004351.1:n.1566-252_1566-251del
NM_001317184.2:c.1383-252_1383-251del NP_001304113.1:n.1383-252_1383-251del
NM_001317185.2:c.18-252_18-251del NP_001304114.1:n.18-252_18-251del
NM_001317186.2:c.-254-2973_-254-2972del NP_001304115.1:n.-254-2973_-254-2972del