Canonical Allele Identifier: CA2633897405
Gene: CDH1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68802017_68802018insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC , CM000678.2:g.68802017_68802018insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC GRCh38
NC_000016.9:g.68835920_68835921insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC , CM000678.1:g.68835920_68835921insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC GRCh37
NC_000016.8:g.67393421_67393422insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC NCBI36
NG_008021.1:g.69726_69727insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC , LRG_301:g.69726_69727insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.387+124_387+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC MANE Select ENSP00000261769.4:n.387+124_387+125insTTACATCTTCAGCAAACTCCCTT...
ENST00000261769.9:c.387+124_387+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC ENSP00000261769.4:n.387+124_387+125insTTACATCTTCAGCAAACTCCCTT...
ENST00000422392.6:c.387+124_387+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC ENSP00000414946.2:n.387+124_387+125insTTACATCTTCAGCAAACTCCCTT...
ENST00000561751.1:c.154+124_154+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC
ENST00000562836.5:n.458+124_458+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC
ENST00000564676.5:n.669+124_669+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC
ENST00000564745.1:n.382+124_382+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC
ENST00000566510.5:c.387+124_387+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC ENSP00000458139.1:n.387+124_387+125insTTACATCTTCAGCAAACTCCCTT...
ENST00000566612.5:c.387+124_387+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC ENSP00000454782.1:n.387+124_387+125insTTACATCTTCAGCAAACTCCCTT...
ENST00000611625.4:c.387+124_387+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC ENSP00000481063.1:n.387+124_387+125insTTACATCTTCAGCAAACTCCCTT...
ENST00000612417.4:c.387+124_387+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC ENSP00000478360.1:n.387+124_387+125insTTACATCTTCAGCAAACTCCCTT...
ENST00000621016.4:c.387+124_387+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC ENSP00000480664.1:n.387+124_387+125insTTACATCTTCAGCAAACTCCCTT...
NM_004360.3:c.387+124_387+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC , LRG_301t1:c.387+124_387+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC NP_004351.1:n.387+124_387+125insTTACATCTTCAGCAAACTCCCTTCTCCTC...
XM_011523488.1:c.-349+124_-349+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC XP_011521790.1:n.-349+124_-349+125insTTACATCTTCAGCAAACTCCCTTC...
XM_011523489.1:c.-349+124_-349+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC XP_011521791.1:n.-349+124_-349+125insTTACATCTTCAGCAAACTCCCTTC...
NM_001317184.1:c.387+124_387+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC NP_001304113.1:n.387+124_387+125insTTACATCTTCAGCAAACTCCCTTCTC...
NM_001317185.1:c.-1229+124_-1229+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC NP_001304114.1:n.-1229+124_-1229+125insTTACATCTTCAGCAAACTCCCT...
NM_001317186.1:c.-1433+124_-1433+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC NP_001304115.1:n.-1433+124_-1433+125insTTACATCTTCAGCAAACTCCCT...
NM_004360.4:c.387+124_387+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC NP_004351.1:n.387+124_387+125insTTACATCTTCAGCAAACTCCCTTCTCCTC...
NM_004360.5:c.387+124_387+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC MANE Select NP_004351.1:n.387+124_387+125insTTACATCTTCAGCAAACTCCCTTCTCCTC...
NM_001317184.2:c.387+124_387+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC NP_001304113.1:n.387+124_387+125insTTACATCTTCAGCAAACTCCCTTCTC...
NM_001317185.2:c.-1229+124_-1229+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC NP_001304114.1:n.-1229+124_-1229+125insTTACATCTTCAGCAAACTCCCT...
NM_001317186.2:c.-1433+124_-1433+125insTTACATCTTCAGCAAACTCCCTTCTCCTCTGC NP_001304115.1:n.-1433+124_-1433+125insTTACATCTTCAGCAAACTCCCT...