Canonical Allele Identifier: CA2633931739
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819221_68819228del , CM000678.2:g.68819221_68819228del GRCh38
NC_000016.9:g.68853124_68853131del , CM000678.1:g.68853124_68853131del GRCh37
NC_000016.8:g.67410625_67410632del NCBI36
NG_008021.1:g.86930_86937del , LRG_301:g.86930_86937del

Transcript Alleles

HGVS Amino-acid change
ENST00000261769.10:c.1566-59_1566-52del MANE Select ENSP00000261769.4:n.1566-59_1566-52del
ENST00000261769.9:c.1566-59_1566-52del ENSP00000261769.4:n.1566-59_1566-52del
ENST00000422392.6:c.1383-59_1383-52del ENSP00000414946.2:n.1383-59_1383-52del
ENST00000562836.5:n.1637-59_1637-52del
ENST00000566510.5:c.*232-59_*232-52del ENSP00000458139.1:n.*232-59_*232-52del
ENST00000566612.5:c.1566-2780_1566-2773del ENSP00000454782.1:n.1566-2780_1566-2773de...
ENST00000611625.4:c.1629-59_1629-52del ENSP00000481063.1:n.1629-59_1629-52del
ENST00000612417.4:c.1566-59_1566-52del ENSP00000478360.1:n.1566-59_1566-52del
ENST00000621016.4:c.1566-59_1566-52del ENSP00000480664.1:n.1566-59_1566-52del
NM_004360.3:c.1566-59_1566-52del , LRG_301t1:c.1566-59_1566-52del NP_004351.1:n.1566-59_1566-52del
XM_011523488.1:c.831-59_831-52del XP_011521790.1:n.831-59_831-52del
XM_011523489.1:c.831-59_831-52del XP_011521791.1:n.831-59_831-52del
NM_001317184.1:c.1383-59_1383-52del NP_001304113.1:n.1383-59_1383-52del
NM_001317185.1:c.18-59_18-52del NP_001304114.1:n.18-59_18-52del
NM_001317186.1:c.-254-2780_-254-2773del NP_001304115.1:n.-254-2780_-254-2773del
NM_004360.4:c.1566-59_1566-52del NP_004351.1:n.1566-59_1566-52del
NM_004360.5:c.1566-59_1566-52del MANE Select NP_004351.1:n.1566-59_1566-52del
NM_001317184.2:c.1383-59_1383-52del NP_001304113.1:n.1383-59_1383-52del
NM_001317185.2:c.18-59_18-52del NP_001304114.1:n.18-59_18-52del
NM_001317186.2:c.-254-2780_-254-2773del NP_001304115.1:n.-254-2780_-254-2773del