Canonical Allele Identifier: CA496152590
Gene: CDH1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.68835584_68835596del (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68801683_68801695del , CM000678.2:g.68801683_68801695del GRCh38
NC_000016.9:g.68835586_68835598del , CM000678.1:g.68835586_68835598del GRCh37
NC_000016.8:g.67393087_67393099del NCBI36
NG_008021.1:g.69392_69404del , LRG_301:g.69392_69404del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.177_189del MANE Select ENSP00000261769.4:p.Cys60LysfsTer19
ENST00000261769.9:c.177_189del ENSP00000261769.4:p.Cys60LysfsTer19
ENST00000422392.6:c.177_189del ENSP00000414946.2:p.Cys60LysfsTer19
ENST00000562836.5:n.248_260del
ENST00000564676.5:n.459_471del
ENST00000564745.1:n.172_184del
ENST00000566510.5:c.177_189del ENSP00000458139.1:p.Cys60LysfsTer19
ENST00000566612.5:c.177_189del ENSP00000454782.1:p.Cys60LysfsTer19
ENST00000611625.4:c.177_189del ENSP00000481063.1:p.Cys60LysfsTer19
ENST00000612417.4:c.177_189del ENSP00000478360.1:p.Cys60LysfsTer19
ENST00000621016.4:c.177_189del ENSP00000480664.1:p.Cys60LysfsTer19
NM_004360.3:c.177_189del , LRG_301t1:c.177_189del NP_004351.1:p.Cys60LysfsTer19
XM_011523488.1:c.-559_-547del XP_011521790.1:n.-559_-547del
XM_011523489.1:c.-559_-547del XP_011521791.1:n.-559_-547del
NM_001317184.1:c.177_189del NP_001304113.1:p.Cys60LysfsTer19
NM_001317185.1:c.-1439_-1427del NP_001304114.1:n.-1439_-1427del
NM_001317186.1:c.-1643_-1631del NP_001304115.1:n.-1643_-1631del
NM_004360.4:c.177_189del NP_004351.1:p.Cys60LysfsTer19
NM_004360.5:c.177_189del MANE Select NP_004351.1:p.Cys60LysfsTer19
NM_001317184.2:c.177_189del NP_001304113.1:p.Cys60LysfsTer19
NM_001317185.2:c.-1439_-1427del NP_001304114.1:n.-1439_-1427del
NM_001317186.2:c.-1643_-1631del NP_001304115.1:n.-1643_-1631del
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