Allele Registry

Canonical Allele Identifier: PA135796

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_005219.2:p.Glu746_Ala750del

CA135794

NM_005228.5:c.2232_2249delinsAAA

CA175996

NM_005228.5:c.2235_2249del

CA175997

NM_005228.5:c.2237_2248delinsCCC

CA180531

NM_005228.5:c.2236_2250del

CA180619

NM_005228.5:c.2235_2248delinsAATTC

CA180653

NM_005228.5:c.2237_2248delinsCAC

CA645561497

NM_005228.5:c.2236_2248delinsCAAC

CA645561513

NM_005228.5:c.2237_2250delinsTCCCT

CA645561522

NM_005228.5:c.2238_2248delinsTC

CA2850447142

NM_005228.5:c.2232_2250delinsTAAG