Canonical Allele Identifier: CA645596628
Gene: CDH1 HGNC NCBI

Linked Data

COSMIC: COSM5029221
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68810259_68810261dup , CM000678.2:g.68810259_68810261dup GRCh38
NC_000016.9:g.68844162_68844164dup , CM000678.1:g.68844162_68844164dup GRCh37
NC_000016.8:g.67401663_67401665dup NCBI36
NG_008021.1:g.77968_77970dup , LRG_301:g.77968_77970dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.750_752dup MANE Select ENSP00000261769.4:p.Thr251_Val252insThr
ENST00000261769.9:c.750_752dup ENSP00000261769.4:p.Thr251_Val252insThr
ENST00000422392.6:c.750_752dup ENSP00000414946.2:p.Thr251_Val252insThr
ENST00000561751.1:c.454+1411_454+1413dup
ENST00000562836.5:n.821_823dup
ENST00000566510.5:c.594_596dup ENSP00000458139.1:p.Thr199_Val200insThr
ENST00000566612.5:c.750_752dup ENSP00000454782.1:p.Thr251_Val252insThr
ENST00000611625.4:c.750_752dup ENSP00000481063.1:p.Thr251_Val252insThr
ENST00000612417.4:c.750_752dup ENSP00000478360.1:p.Thr251_Val252insThr
ENST00000621016.4:c.750_752dup ENSP00000480664.1:p.Thr251_Val252insThr
NM_004360.3:c.750_752dup , LRG_301t1:c.750_752dup NP_004351.1:p.Thr251_Val252insThr
XM_011523488.1:c.15_17dup XP_011521790.1:p.Thr6_Val7insThr
XM_011523489.1:c.15_17dup XP_011521791.1:p.Thr6_Val7insThr
NM_001317184.1:c.750_752dup NP_001304113.1:p.Thr251_Val252insThr
NM_001317185.1:c.-866_-864dup NP_001304114.1:n.-866_-864dup
NM_001317186.1:c.-1070_-1068dup NP_001304115.1:n.-1070_-1068dup
NM_004360.4:c.750_752dup NP_004351.1:p.Thr251_Val252insThr
NM_004360.5:c.750_752dup MANE Select NP_004351.1:p.Thr251_Val252insThr
NM_001317184.2:c.750_752dup NP_001304113.1:p.Thr251_Val252insThr
NM_001317185.2:c.-866_-864dup NP_001304114.1:n.-866_-864dup
NM_001317186.2:c.-1070_-1068dup NP_001304115.1:n.-1070_-1068dup
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