Canonical Allele Identifier: CA2580091855
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1723384
ClinVar RCV Id: RCV002308660

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833272_68833280del , CM000678.2:g.68833272_68833280del GRCh38
NC_000016.9:g.68867175_68867183del , CM000678.1:g.68867175_68867183del GRCh37
NC_000016.8:g.67424676_67424684del NCBI36
NG_008021.1:g.100981_100989del , LRG_301:g.100981_100989del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2440-18_2440-10del MANE Select ENSP00000261769.4:n.2440-18_2440-10del
ENST00000261769.9:c.2440-18_2440-10del ENSP00000261769.4:n.2440-18_2440-10del
ENST00000422392.6:c.2257-18_2257-10del ENSP00000414946.2:n.2257-18_2257-10del
ENST00000562118.1:n.658-18_658-10del
ENST00000562836.5:n.2511-18_2511-10del
ENST00000566510.5:c.*1106-18_*1106-10del ENSP00000458139.1:n.*1106-18_*1106-10del
ENST00000566612.5:c.*680-18_*680-10del ENSP00000454782.1:n.*680-18_*680-10del
ENST00000611625.4:c.2503-18_2503-10del ENSP00000481063.1:n.2503-18_2503-10del
ENST00000612417.4:c.1854-919_1854-911del ENSP00000478360.1:n.1854-919_1854-911del
ENST00000621016.4:c.1866-931_1866-923del ENSP00000480664.1:n.1866-931_1866-923del
NM_004360.3:c.2440-18_2440-10del , LRG_301t1:c.2440-18_2440-10del NP_004351.1:n.2440-18_2440-10del
XM_011523488.1:c.1705-18_1705-10del XP_011521790.1:n.1705-18_1705-10del
XM_011523489.1:c.1705-18_1705-10del XP_011521791.1:n.1705-18_1705-10del
NM_001317184.1:c.2257-18_2257-10del NP_001304113.1:n.2257-18_2257-10del
NM_001317185.1:c.892-18_892-10del NP_001304114.1:n.892-18_892-10del
NM_001317186.1:c.475-18_475-10del NP_001304115.1:n.475-18_475-10del
NM_004360.4:c.2440-18_2440-10del NP_004351.1:n.2440-18_2440-10del
NM_004360.5:c.2440-18_2440-10del MANE Select NP_004351.1:n.2440-18_2440-10del
NM_001317184.2:c.2257-18_2257-10del NP_001304113.1:n.2257-18_2257-10del
NM_001317185.2:c.892-18_892-10del NP_001304114.1:n.892-18_892-10del
NM_001317186.2:c.475-18_475-10del NP_001304115.1:n.475-18_475-10del