Canonical Allele Identifier: CA2229978731
Gene: CDH1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833528_68833529delinsCA , CM000678.2:g.68833528_68833529delinsCA GRCh38
NC_000016.9:g.68867431_68867432delinsCA , CM000678.1:g.68867431_68867432delinsCA GRCh37
NC_000016.8:g.67424932_67424933delinsCA NCBI36
NG_008021.1:g.101237_101238delinsCA , LRG_301:g.101237_101238delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.*29_*30delinsCA MANE Select ENSP00000261769.4:n.*29_*30delinsCA
ENST00000261769.9:c.*29_*30delinsCA ENSP00000261769.4:n.*29_*30delinsCA
ENST00000422392.6:c.*29_*30delinsCA ENSP00000414946.2:n.*29_*30delinsCA
ENST00000562118.1:n.896_897delinsCA
ENST00000562836.5:n.2749_2750delinsCA
ENST00000566510.5:c.*1344_*1345delinsCA ENSP00000458139.1:n.*1344_*1345delinsCA
ENST00000566612.5:c.*918_*919delinsCA ENSP00000454782.1:n.*918_*919delinsCA
ENST00000611625.4:c.*29_*30delinsCA ENSP00000481063.1:n.*29_*30delinsCA
ENST00000612417.4:c.1854-663_1854-662delinsCA ENSP00000478360.1:n.1854-663_1854-662delinsCA
ENST00000621016.4:c.1866-675_1866-674delinsCA ENSP00000480664.1:n.1866-675_1866-674delinsCA
NM_004360.3:c.*29_*30delinsCA , LRG_301t1:c.*29_*30delinsCA NP_004351.1:n.*29_*30delinsCA
XM_011523488.1:c.*29_*30delinsCA XP_011521790.1:n.*29_*30delinsCA
XM_011523489.1:c.*29_*30delinsCA XP_011521791.1:n.*29_*30delinsCA
NM_001317184.1:c.*29_*30delinsCA NP_001304113.1:n.*29_*30delinsCA
NM_001317185.1:c.*29_*30delinsCA NP_001304114.1:n.*29_*30delinsCA
NM_001317186.1:c.*29_*30delinsCA NP_001304115.1:n.*29_*30delinsCA
NM_004360.4:c.*29_*30delinsCA NP_004351.1:n.*29_*30delinsCA
NM_004360.5:c.*29_*30delinsCA MANE Select NP_004351.1:n.*29_*30delinsCA
NM_001317184.2:c.*29_*30delinsCA NP_001304113.1:n.*29_*30delinsCA
NM_001317185.2:c.*29_*30delinsCA NP_001304114.1:n.*29_*30delinsCA
NM_001317186.2:c.*29_*30delinsCA NP_001304115.1:n.*29_*30delinsCA
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