Canonical Allele Identifier: CA1139664741
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 968651
ClinVar RCV Id: RCV001243837
dbSNP Id: rs1962425092
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68737444delinsGGCT , CM000678.2:g.68737444delinsGGCT GRCh38
NC_000016.9:g.68771347delinsGGCT , CM000678.1:g.68771347delinsGGCT GRCh37
NC_000016.8:g.67328848delinsGGCT NCBI36
NG_008021.1:g.5153delinsGGCT , LRG_301:g.5153delinsGGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.29delinsGGCT MANE Select ENSP00000261769.4:p.Ala10delinsGlyLeu
ENST00000261769.9:c.29delinsGGCT ENSP00000261769.4:p.Ala10delinsGlyLeu
ENST00000422392.6:c.29delinsGGCT ENSP00000414946.2:p.Ala10delinsGlyLeu
ENST00000566510.5:c.29delinsGGCT ENSP00000458139.1:p.Ala10delinsGlyLeu
ENST00000566612.5:c.29delinsGGCT ENSP00000454782.1:p.Ala10delinsGlyLeu
ENST00000611625.4:c.29delinsGGCT ENSP00000481063.1:p.Ala10delinsGlyLeu
ENST00000612417.4:c.29delinsGGCT ENSP00000478360.1:p.Ala10delinsGlyLeu
ENST00000621016.4:c.29delinsGGCT ENSP00000480664.1:p.Ala10delinsGlyLeu
NM_004360.3:c.29delinsGGCT , LRG_301t1:c.29delinsGGCT NP_004351.1:p.Ala10delinsGlyLeu
NM_001317184.1:c.29delinsGGCT NP_001304113.1:p.Ala10delinsGlyLeu
NM_001317185.1:c.-1587delinsGGCT NP_001304114.1:n.-1587delinsGGCT
NM_001317186.1:c.-1791delinsGGCT NP_001304115.1:n.-1791delinsGGCT
NM_004360.4:c.29delinsGGCT NP_004351.1:p.Ala10delinsGlyLeu
NM_004360.5:c.29delinsGGCT MANE Select NP_004351.1:p.Ala10delinsGlyLeu
NM_001317184.2:c.29delinsGGCT NP_001304113.1:p.Ala10delinsGlyLeu
NM_001317185.2:c.-1587delinsGGCT NP_001304114.1:n.-1587delinsGGCT
NM_001317186.2:c.-1791delinsGGCT NP_001304115.1:n.-1791delinsGGCT
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