Allele Registry

Canonical Allele Identifier: PA2827395189

Gene: EGFR HGNC NCBI

Linked Data

ClinVar Variation Id: 45233

ClinVar RCV Id: RCV000038389

ClinVar Variation Id: 163343

ClinVar RCV Id: RCV000150617 RCV002514895 RCV003128584

ClinVar Variation Id: 177620

ClinVar RCV Id: RCV000154199 RCV001311279 RCV003998240

Amino-acid Alleles

HGVS (amino-acid)

Matching Registered Transcripts

NP_001333870.1:p.Glu479_Ala483del

CA135794

NM_001346941.2:c.1431_1448delinsAAA

CA175996

NM_001346941.2:c.1434_1448del

CA175997

NM_001346941.2:c.1436_1447delinsCCC

CA180531

NM_001346941.2:c.1435_1449del

CA180619

NM_001346941.2:c.1434_1447delinsAATTC

CA180653

NM_001346941.2:c.1436_1447delinsCAC

CA645561497

NM_001346941.2:c.1435_1447delinsCAAC

CA645561513

NM_001346941.2:c.1436_1449delinsTCCCT

CA645561522

NM_001346941.2:c.1437_1447delinsTC

CA2850447142

NM_001346941.2:c.1431_1449delinsTAAG