Canonical Allele Identifier: CA919732172
Gene: CDH1 HGNC NCBI

Linked Data

dbSNP Id: rs5817654
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810572_68810580dup , CM000678.2:g.68810572_68810580dup GRCh38
NC_000016.9:g.68844475_68844483dup , CM000678.1:g.68844475_68844483dup GRCh37
NC_000016.8:g.67401976_67401984dup NCBI36
NG_008021.1:g.78281_78289dup , LRG_301:g.78281_78289dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.832+231_832+239dup MANE Select ENSP00000261769.4:n.832+231_832+239dup
ENST00000261769.9:c.832+231_832+239dup ENSP00000261769.4:n.832+231_832+239dup
ENST00000422392.6:c.832+231_832+239dup ENSP00000414946.2:n.832+231_832+239dup
ENST00000561751.1:c.455-1112_455-1104dup
ENST00000562836.5:n.903+231_903+239dup
ENST00000566510.5:c.676+231_676+239dup ENSP00000458139.1:n.676+231_676+239dup
ENST00000566612.5:c.832+231_832+239dup ENSP00000454782.1:n.832+231_832+239dup
ENST00000611625.4:c.832+231_832+239dup ENSP00000481063.1:n.832+231_832+239dup
ENST00000612417.4:c.832+231_832+239dup ENSP00000478360.1:n.832+231_832+239dup
ENST00000621016.4:c.832+231_832+239dup ENSP00000480664.1:n.832+231_832+239dup
NM_004360.3:c.832+231_832+239dup , LRG_301t1:c.832+231_832+239dup NP_004351.1:n.832+231_832+239dup
XM_011523488.1:c.97+231_97+239dup XP_011521790.1:n.97+231_97+239dup
XM_011523489.1:c.97+231_97+239dup XP_011521791.1:n.97+231_97+239dup
NM_001317184.1:c.832+231_832+239dup NP_001304113.1:n.832+231_832+239dup
NM_001317185.1:c.-784+231_-784+239dup NP_001304114.1:n.-784+231_-784+239dup
NM_001317186.1:c.-988+231_-988+239dup NP_001304115.1:n.-988+231_-988+239dup
NM_004360.4:c.832+231_832+239dup NP_004351.1:n.832+231_832+239dup
NM_004360.5:c.832+231_832+239dup MANE Select NP_004351.1:n.832+231_832+239dup
NM_001317184.2:c.832+231_832+239dup NP_001304113.1:n.832+231_832+239dup
NM_001317185.2:c.-784+231_-784+239dup NP_001304114.1:n.-784+231_-784+239dup
NM_001317186.2:c.-988+231_-988+239dup NP_001304115.1:n.-988+231_-988+239dup
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