Canonical Allele Identifier: CA2229958269
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1960528080
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68801926_68801941del , CM000678.2:g.68801926_68801941del GRCh38
NC_000016.9:g.68835829_68835844del , CM000678.1:g.68835829_68835844del GRCh37
NC_000016.8:g.67393330_67393345del NCBI36
NG_008021.1:g.69635_69650del , LRG_301:g.69635_69650del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.387+33_387+48del MANE Select ENSP00000261769.4:n.387+33_387+48del
ENST00000261769.9:c.387+33_387+48del ENSP00000261769.4:n.387+33_387+48del
ENST00000422392.6:c.387+33_387+48del ENSP00000414946.2:n.387+33_387+48del
ENST00000561751.1:c.154+33_154+48del
ENST00000562836.5:n.458+33_458+48del
ENST00000564676.5:n.669+33_669+48del
ENST00000564745.1:n.382+33_382+48del
ENST00000566510.5:c.387+33_387+48del ENSP00000458139.1:n.387+33_387+48del
ENST00000566612.5:c.387+33_387+48del ENSP00000454782.1:n.387+33_387+48del
ENST00000611625.4:c.387+33_387+48del ENSP00000481063.1:n.387+33_387+48del
ENST00000612417.4:c.387+33_387+48del ENSP00000478360.1:n.387+33_387+48del
ENST00000621016.4:c.387+33_387+48del ENSP00000480664.1:n.387+33_387+48del
NM_004360.3:c.387+33_387+48del , LRG_301t1:c.387+33_387+48del NP_004351.1:n.387+33_387+48del
XM_011523488.1:c.-349+33_-349+48del XP_011521790.1:n.-349+33_-349+48del
XM_011523489.1:c.-349+33_-349+48del XP_011521791.1:n.-349+33_-349+48del
NM_001317184.1:c.387+33_387+48del NP_001304113.1:n.387+33_387+48del
NM_001317185.1:c.-1229+33_-1229+48del NP_001304114.1:n.-1229+33_-1229+48del
NM_001317186.1:c.-1433+33_-1433+48del NP_001304115.1:n.-1433+33_-1433+48del
NM_004360.4:c.387+33_387+48del NP_004351.1:n.387+33_387+48del
NM_004360.5:c.387+33_387+48del MANE Select NP_004351.1:n.387+33_387+48del
NM_001317184.2:c.387+33_387+48del NP_001304113.1:n.387+33_387+48del
NM_001317185.2:c.-1229+33_-1229+48del NP_001304114.1:n.-1229+33_-1229+48del
NM_001317186.2:c.-1433+33_-1433+48del NP_001304115.1:n.-1433+33_-1433+48del
Search 100 bp 5'
Search 100 bp 3'