Allele Registry

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Canonical Allele Identifier: PA2827393322

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

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Amino-acid Alleles

HGVS (amino-acid)

Matching Registered Transcripts

NP_001333829.1:p.Glu693_Ala697del

CA135794

NM_001346900.1:c.2073_2090delinsAAA

CA175996

NM_001346900.1:c.2076_2090del

CA175997

NM_001346900.1:c.2078_2089delinsCCC

CA180531

NM_001346900.1:c.2077_2091del

CA180619

NM_001346900.1:c.2076_2089delinsAATTC

CA180653

NM_001346900.1:c.2078_2089delinsCAC

CA645561497

NM_001346900.1:c.2077_2089delinsCAAC

CA645561513

NM_001346900.1:c.2078_2091delinsTCCCT

CA645561522

NM_001346900.1:c.2079_2089delinsTC