Canonical Allele Identifier: CA496157505
Gene: CDH1 HGNC NCBI

Linked Data

COSMIC: COSM19509
MyVariant Identifiers: chr16:g.68863671del (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68829770del , CM000678.2:g.68829770del GRCh38
NC_000016.9:g.68863673del , CM000678.1:g.68863673del GRCh37
NC_000016.8:g.67421174del NCBI36
NG_008021.1:g.97479del , LRG_301:g.97479del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2412del MANE Select ENSP00000261769.4:p.Asp805MetfsTer11
ENST00000261769.9:c.2412del ENSP00000261769.4:p.Asp805MetfsTer11
ENST00000422392.6:c.2229del ENSP00000414946.2:p.Asp744MetfsTer11
ENST00000562118.1:n.630del
ENST00000562836.5:n.2483del
ENST00000566510.5:c.*1078del ENSP00000458139.1:n.*1078del
ENST00000566612.5:c.*652del ENSP00000454782.1:n.*652del
ENST00000611625.4:c.2475del ENSP00000481063.1:p.Asp826MetfsTer11
ENST00000612417.4:c.1853+3216del ENSP00000478360.1:n.1853+3216del
ENST00000621016.4:c.1866-4433del ENSP00000480664.1:n.1866-4433del
NM_004360.3:c.2412del , LRG_301t1:c.2412del NP_004351.1:p.Asp805MetfsTer11
XM_011523488.1:c.1677del XP_011521790.1:p.Asp560MetfsTer11
XM_011523489.1:c.1677del XP_011521791.1:p.Asp560MetfsTer11
NM_001317184.1:c.2229del NP_001304113.1:p.Asp744MetfsTer11
NM_001317185.1:c.864del NP_001304114.1:p.Asp289MetfsTer11
NM_001317186.1:c.447del NP_001304115.1:p.Asp150MetfsTer11
NM_004360.4:c.2412del NP_004351.1:p.Asp805MetfsTer11
NM_004360.5:c.2412del MANE Select NP_004351.1:p.Asp805MetfsTer11
NM_001317184.2:c.2229del NP_001304113.1:p.Asp744MetfsTer11
NM_001317185.2:c.864del NP_001304114.1:p.Asp289MetfsTer11
NM_001317186.2:c.447del NP_001304115.1:p.Asp150MetfsTer11
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