Canonical Allele Identifier: CA645596591
Gene: CDH1 HGNC NCBI

Linked Data

COSMIC: COSM19525
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.68801754_68801755insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT , CM000678.2:g.68801754_68801755insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT GRCh38
NC_000016.9:g.68835657_68835658insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT , CM000678.1:g.68835657_68835658insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT GRCh37
NC_000016.8:g.67393158_67393159insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT NCBI36
NG_008021.1:g.69463_69464insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT , LRG_301:g.69463_69464insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261769.10:c.248_249insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT MANE Select ENSP00000261769.4:p.Thr84ProfsTer?
ENST00000261769.9:c.248_249insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT ENSP00000261769.4:p.Thr84ProfsTer?
ENST00000422392.6:c.248_249insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT ENSP00000414946.2:p.Thr84ProfsTer?
ENST00000561751.1:c.15_16insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT
ENST00000562836.5:n.319_320insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT
ENST00000564676.5:n.530_531insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT
ENST00000564745.1:n.243_244insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT
ENST00000566510.5:c.248_249insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT ENSP00000458139.1:p.Thr84ProfsTer?
ENST00000566612.5:c.248_249insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT ENSP00000454782.1:p.Thr84ProfsTer?
ENST00000611625.4:c.248_249insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT ENSP00000481063.1:p.Thr84ProfsTer?
ENST00000612417.4:c.248_249insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT ENSP00000478360.1:p.Thr84ProfsTer?
ENST00000621016.4:c.248_249insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT ENSP00000480664.1:p.Thr84ProfsTer?
NM_004360.3:c.248_249insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT , LRG_301t1:c.248_249insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT NP_004351.1:p.Thr84ProfsTer?
XM_011523488.1:c.-488_-487insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT XP_011521790.1:n.-488_-487insCCCTCGACACCCGATTCAAAGTGGGCACAGAT...
XM_011523489.1:c.-488_-487insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT XP_011521791.1:n.-488_-487insCCCTCGACACCCGATTCAAAGTGGGCACAGAT...
NM_001317184.1:c.248_249insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT NP_001304113.1:p.Thr84ProfsTer?
NM_001317185.1:c.-1368_-1367insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT NP_001304114.1:n.-1368_-1367insCCCTCGACACCCGATTCAAAGTGGGCACAG...
NM_001317186.1:c.-1572_-1571insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT NP_001304115.1:n.-1572_-1571insCCCTCGACACCCGATTCAAAGTGGGCACAG...
NM_004360.4:c.248_249insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT NP_004351.1:p.Thr84ProfsTer?
NM_004360.5:c.248_249insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT MANE Select NP_004351.1:p.Thr84ProfsTer?
NM_001317184.2:c.248_249insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT NP_001304113.1:p.Thr84ProfsTer?
NM_001317185.2:c.-1368_-1367insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT NP_001304114.1:n.-1368_-1367insCCCTCGACACCCGATTCAAAGTGGGCACAG...
NM_001317186.2:c.-1572_-1571insCCCTCGACACCCGATTCAAAGTGGGCACAGATGGTGTGATT NP_001304115.1:n.-1572_-1571insCCCTCGACACCCGATTCAAAGTGGGCACAG...
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