Canonical Allele Identifier: CA978529393
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs1003174610
gnomAD v3: 16-68832821-TA-T
gnomAD v4: 16-68832821-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68832830del , CM000678.2:g.68832830del GRCh38
NC_000016.9:g.68866733del , CM000678.1:g.68866733del GRCh37
NC_000016.8:g.67424234del NCBI36
NG_008021.1:g.100539del , LRG_301:g.100539del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2440-460del MANE Select ENSP00000261769.4:n.2440-460del
ENST00000261769.9:c.2440-460del ENSP00000261769.4:n.2440-460del
ENST00000422392.6:c.2257-460del ENSP00000414946.2:n.2257-460del
ENST00000562118.1:n.658-460del
ENST00000562836.5:n.2511-460del
ENST00000566510.5:c.*1106-460del ENSP00000458139.1:n.*1106-460del
ENST00000566612.5:c.*680-460del ENSP00000454782.1:n.*680-460del
ENST00000611625.4:c.2503-460del ENSP00000481063.1:n.2503-460del
ENST00000612417.4:c.1854-1361del ENSP00000478360.1:n.1854-1361del
ENST00000621016.4:c.1866-1373del ENSP00000480664.1:n.1866-1373del
NM_004360.3:c.2440-460del , LRG_301t1:c.2440-460del NP_004351.1:n.2440-460del
XM_011523488.1:c.1705-460del XP_011521790.1:n.1705-460del
XM_011523489.1:c.1705-460del XP_011521791.1:n.1705-460del
NM_001317184.1:c.2257-460del NP_001304113.1:n.2257-460del
NM_001317185.1:c.892-460del NP_001304114.1:n.892-460del
NM_001317186.1:c.475-460del NP_001304115.1:n.475-460del
NM_004360.4:c.2440-460del NP_004351.1:n.2440-460del
NM_004360.5:c.2440-460del MANE Select NP_004351.1:n.2440-460del
NM_001317184.2:c.2257-460del NP_001304113.1:n.2257-460del
NM_001317185.2:c.892-460del NP_001304114.1:n.892-460del
NM_001317186.2:c.475-460del NP_001304115.1:n.475-460del
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