Canonical Allele Identifier: CA367580281
Gene: EGFR HGNC NCBI

Linked Data

COSMIC: COSM85994

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55191825C>A , CM000669.2:g.55191825C>A GRCh38
NC_000007.13:g.55259518C>A , CM000669.1:g.55259518C>A GRCh37
NC_000007.12:g.55227012C>A NCBI36
NG_007726.3:g.177794C>A , LRG_304:g.177794C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000275493.7:c.2576C>A MANE Select ENSP00000275493.2:p.Ala859Asp
ENST00000275493.6:c.2576C>A ENSP00000275493.2:p.Ala859Asp
ENST00000442591.5:c.*28+18897C>A ENSP00000410031.1:n.*28+18897C>A
ENST00000454757.6:c.2441C>A ENSP00000395243.3:p.Ala814Asp
ENST00000455089.5:c.2441C>A ENSP00000415559.1:p.Ala814Asp
NM_005228.3:c.2576C>A , LRG_304t1:c.2576C>A NP_005219.2:p.Ala859Asp
NM_001346897.1:c.2441C>A NP_001333826.1:p.Ala814Asp
NM_001346898.1:c.2576C>A NP_001333827.1:p.Ala859Asp
NM_001346899.1:c.2441C>A NP_001333828.1:p.Ala814Asp
NM_001346900.1:c.2417C>A NP_001333829.1:p.Ala806Asp
NM_001346941.1:c.1775C>A NP_001333870.1:p.Ala592Asp
NM_005228.4:c.2576C>A NP_005219.2:p.Ala859Asp
NM_005228.5:c.2576C>A MANE Select NP_005219.2:p.Ala859Asp
NM_001346897.2:c.2441C>A NP_001333826.1:p.Ala814Asp
NM_001346898.2:c.2576C>A NP_001333827.1:p.Ala859Asp
NM_001346900.2:c.2417C>A NP_001333829.1:p.Ala806Asp
NM_001346941.2:c.1775C>A NP_001333870.1:p.Ala592Asp
NM_001346899.2:c.2441C>A NP_001333828.1:p.Ala814Asp