Canonical Allele Identifier: CA2229977478
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1961065764

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68819092_68819109dup , CM000678.2:g.68819092_68819109dup GRCh38
NC_000016.9:g.68852995_68853012dup , CM000678.1:g.68852995_68853012dup GRCh37
NC_000016.8:g.67410496_67410513dup NCBI36
NG_008021.1:g.86801_86818dup , LRG_301:g.86801_86818dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.1566-188_1566-171dup MANE Select ENSP00000261769.4:n.1566-188_1566-171dup
ENST00000261769.9:c.1566-188_1566-171dup ENSP00000261769.4:n.1566-188_1566-171dup
ENST00000422392.6:c.1383-188_1383-171dup ENSP00000414946.2:n.1383-188_1383-171dup
ENST00000562836.5:n.1637-188_1637-171dup
ENST00000566510.5:c.*232-188_*232-171dup ENSP00000458139.1:n.*232-188_*232-171dup
ENST00000566612.5:c.1566-2909_1566-2892dup ENSP00000454782.1:n.1566-2909_1566-2892dup
ENST00000611625.4:c.1629-188_1629-171dup ENSP00000481063.1:n.1629-188_1629-171dup
ENST00000612417.4:c.1566-188_1566-171dup ENSP00000478360.1:n.1566-188_1566-171dup
ENST00000621016.4:c.1566-188_1566-171dup ENSP00000480664.1:n.1566-188_1566-171dup
NM_004360.3:c.1566-188_1566-171dup , LRG_301t1:c.1566-188_1566-171dup NP_004351.1:n.1566-188_1566-171dup
XM_011523488.1:c.831-188_831-171dup XP_011521790.1:n.831-188_831-171dup
XM_011523489.1:c.831-188_831-171dup XP_011521791.1:n.831-188_831-171dup
NM_001317184.1:c.1383-188_1383-171dup NP_001304113.1:n.1383-188_1383-171dup
NM_001317185.1:c.18-188_18-171dup NP_001304114.1:n.18-188_18-171dup
NM_001317186.1:c.-254-2909_-254-2892dup NP_001304115.1:n.-254-2909_-254-2892dup
NM_004360.4:c.1566-188_1566-171dup NP_004351.1:n.1566-188_1566-171dup
NM_004360.5:c.1566-188_1566-171dup MANE Select NP_004351.1:n.1566-188_1566-171dup
NM_001317184.2:c.1383-188_1383-171dup NP_001304113.1:n.1383-188_1383-171dup
NM_001317185.2:c.18-188_18-171dup NP_001304114.1:n.18-188_18-171dup
NM_001317186.2:c.-254-2909_-254-2892dup NP_001304115.1:n.-254-2909_-254-2892dup