Canonical Allele Identifier: CA2229978202
Gene: CDH1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68833375_68833376delinsCT , CM000678.2:g.68833375_68833376delinsCT GRCh38
NC_000016.9:g.68867278_68867279delinsCT , CM000678.1:g.68867278_68867279delinsCT GRCh37
NC_000016.8:g.67424779_67424780delinsCT NCBI36
NG_008021.1:g.101084_101085delinsCT , LRG_301:g.101084_101085delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.2525_2526delinsCT MANE Select ENSP00000261769.4:p.Ala842=
ENST00000261769.9:c.2525_2526delinsCT ENSP00000261769.4:p.Ala842=
ENST00000422392.6:c.2342_2343delinsCT ENSP00000414946.2:p.Ala781=
ENST00000562118.1:n.743_744delinsCT
ENST00000562836.5:n.2596_2597delinsCT
ENST00000566510.5:c.*1191_*1192delinsCT ENSP00000458139.1:n.*1191_*1192delinsCT
ENST00000566612.5:c.*765_*766delinsCT ENSP00000454782.1:n.*765_*766delinsCT
ENST00000611625.4:c.2588_2589delinsCT ENSP00000481063.1:p.Ala863=
ENST00000612417.4:c.1854-816_1854-815delinsCT ENSP00000478360.1:n.1854-816_1854-815delinsCT
ENST00000621016.4:c.1866-828_1866-827delinsCT ENSP00000480664.1:n.1866-828_1866-827delinsCT
NM_004360.3:c.2525_2526delinsCT , LRG_301t1:c.2525_2526delinsCT NP_004351.1:p.Ala842=
XM_011523488.1:c.1790_1791delinsCT XP_011521790.1:p.Ala597=
XM_011523489.1:c.1790_1791delinsCT XP_011521791.1:p.Ala597=
NM_001317184.1:c.2342_2343delinsCT NP_001304113.1:p.Ala781=
NM_001317185.1:c.977_978delinsCT NP_001304114.1:p.Ala326=
NM_001317186.1:c.560_561delinsCT NP_001304115.1:p.Ala187=
NM_004360.4:c.2525_2526delinsCT NP_004351.1:p.Ala842=
NM_004360.5:c.2525_2526delinsCT MANE Select NP_004351.1:p.Ala842=
NM_001317184.2:c.2342_2343delinsCT NP_001304113.1:p.Ala781=
NM_001317185.2:c.977_978delinsCT NP_001304114.1:p.Ala326=
NM_001317186.2:c.560_561delinsCT NP_001304115.1:p.Ala187=
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