Canonical Allele Identifier: PA2827391548
Gene: EGFR HGNC NCBI

Linked Data

ClinVar Variation Id: 45233
ClinVar RCV Id: RCV000038389
ClinVar Variation Id: 163343
ClinVar Variation Id: 177620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333828.1:p.Glu701_Ala705del
CA135794
NM_001346899.1:c.2097_2114delinsAAA
CA175996
NM_001346899.1:c.2100_2114del
CA175997
NM_001346899.1:c.2102_2113delinsCCC
CA180531
NM_001346899.1:c.2101_2115del
CA180619
NM_001346899.1:c.2100_2113delinsAATTC
CA180653
NM_001346899.1:c.2102_2113delinsCAC
CA645561497
NM_001346899.1:c.2101_2113delinsCAAC
CA645561513
NM_001346899.1:c.2102_2115delinsTCCCT
CA645561522
NM_001346899.1:c.2103_2113delinsTC
CA2850447142
NM_001346899.1:c.2097_2115delinsTAAG