Canonical Allele Identifier: CA658658500
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 481173
dbSNP Id: rs1555518236

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833355_68833356dup , CM000678.2:g.68833355_68833356dup GRCh38
NC_000016.9:g.68867258_68867259dup , CM000678.1:g.68867258_68867259dup GRCh37
NC_000016.8:g.67424759_67424760dup NCBI36
NG_008021.1:g.101064_101065dup , LRG_301:g.101064_101065dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2505_2506dup MANE Select ENSP00000261769.4:p.Glu836ValfsTer11
ENST00000261769.9:c.2505_2506dup ENSP00000261769.4:p.Glu836ValfsTer11
ENST00000422392.6:c.2322_2323dup ENSP00000414946.2:p.Glu775ValfsTer11
ENST00000562118.1:n.723_724dup
ENST00000562836.5:n.2576_2577dup
ENST00000566510.5:c.*1171_*1172dup ENSP00000458139.1:n.*1171_*1172dup
ENST00000566612.5:c.*745_*746dup ENSP00000454782.1:n.*745_*746dup
ENST00000611625.4:c.2568_2569dup ENSP00000481063.1:p.Glu857ValfsTer11
ENST00000612417.4:c.1854-836_1854-835dup ENSP00000478360.1:n.1854-836_1854-835dup
ENST00000621016.4:c.1866-848_1866-847dup ENSP00000480664.1:n.1866-848_1866-847dup
NM_004360.3:c.2505_2506dup , LRG_301t1:c.2505_2506dup NP_004351.1:p.Glu836ValfsTer11
XM_011523488.1:c.1770_1771dup XP_011521790.1:p.Glu591ValfsTer11
XM_011523489.1:c.1770_1771dup XP_011521791.1:p.Glu591ValfsTer11
NM_001317184.1:c.2322_2323dup NP_001304113.1:p.Glu775ValfsTer11
NM_001317185.1:c.957_958dup NP_001304114.1:p.Glu320ValfsTer11
NM_001317186.1:c.540_541dup NP_001304115.1:p.Glu181ValfsTer11
NM_004360.4:c.2505_2506dup NP_004351.1:p.Glu836ValfsTer11
NM_004360.5:c.2505_2506dup MANE Select NP_004351.1:p.Glu836ValfsTer11
NM_001317184.2:c.2322_2323dup NP_001304113.1:p.Glu775ValfsTer11
NM_001317185.2:c.957_958dup NP_001304114.1:p.Glu320ValfsTer11
NM_001317186.2:c.540_541dup NP_001304115.1:p.Glu181ValfsTer11