Canonical Allele Identifier: CA2633899882
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810357_68810358insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG , CM000678.2:g.68810357_68810358insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG GRCh38
NC_000016.9:g.68844260_68844261insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG , CM000678.1:g.68844260_68844261insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG GRCh37
NC_000016.8:g.67401761_67401762insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG NCBI36
NG_008021.1:g.78066_78067insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG , LRG_301:g.78066_78067insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG MANE Select ENSP00000261769.4:n.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCT...
ENST00000261769.9:c.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG ENSP00000261769.4:n.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCT...
ENST00000422392.6:c.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG ENSP00000414946.2:n.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCT...
ENST00000561751.1:c.455-1327_455-1326insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG
ENST00000562836.5:n.903+16_903+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG
ENST00000566510.5:c.676+16_676+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG ENSP00000458139.1:n.676+16_676+17insACCCTCACTTGGTTCTTTCAGCTCT...
ENST00000566612.5:c.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG ENSP00000454782.1:n.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCT...
ENST00000611625.4:c.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG ENSP00000481063.1:n.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCT...
ENST00000612417.4:c.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG ENSP00000478360.1:n.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCT...
ENST00000621016.4:c.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG ENSP00000480664.1:n.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCT...
NM_004360.3:c.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG , LRG_301t1:c.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG NP_004351.1:n.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTC...
XM_011523488.1:c.97+16_97+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG XP_011521790.1:n.97+16_97+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCT...
XM_011523489.1:c.97+16_97+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG XP_011521791.1:n.97+16_97+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCT...
NM_001317184.1:c.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG NP_001304113.1:n.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCTTCT...
NM_001317185.1:c.-784+16_-784+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG NP_001304114.1:n.-784+16_-784+17insACCCTCACTTGGTTCTTTCAGCTCTT...
NM_001317186.1:c.-988+16_-988+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG NP_001304115.1:n.-988+16_-988+17insACCCTCACTTGGTTCTTTCAGCTCTT...
NM_004360.4:c.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG NP_004351.1:n.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTC...
NM_004360.5:c.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG MANE Select NP_004351.1:n.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTC...
NM_001317184.2:c.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG NP_001304113.1:n.832+16_832+17insACCCTCACTTGGTTCTTTCAGCTCTTCT...
NM_001317185.2:c.-784+16_-784+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG NP_001304114.1:n.-784+16_-784+17insACCCTCACTTGGTTCTTTCAGCTCTT...
NM_001317186.2:c.-988+16_-988+17insACCCTCACTTGGTTCTTTCAGCTCTTCTCTCACGCTGTGTCATCCAACGG NP_001304115.1:n.-988+16_-988+17insACCCTCACTTGGTTCTTTCAGCTCTT...