Canonical Allele Identifier: CA16602542
Gene: EGFR HGNC NCBI

Linked Data

ClinVar Variation Id: 376080
ClinVar RCV Id: RCV000433245
dbSNP Id: rs121913433
COSMIC: COSM14243

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174771A>G , CM000669.2:g.55174771A>G GRCh38
NC_000007.13:g.55242464A>G , CM000669.1:g.55242464A>G GRCh37
NC_000007.12:g.55209958A>G NCBI36
NG_007726.3:g.160740A>G , LRG_304:g.160740A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2075A>G ENSP00000413354.2:p.Lys692Arg
ENST00000700145.1:c.583A>G
ENST00000275493.7:c.2234A>G MANE Select ENSP00000275493.2:p.Lys745Arg
ENST00000275493.6:c.2234A>G ENSP00000275493.2:p.Lys745Arg
ENST00000442591.5:c.*28+1843A>G ENSP00000410031.1:n.*28+1843A>G
ENST00000454757.6:c.2099A>G ENSP00000395243.3:p.Lys700Arg
ENST00000455089.5:c.2099A>G ENSP00000415559.1:p.Lys700Arg
NM_005228.3:c.2234A>G , LRG_304t1:c.2234A>G NP_005219.2:p.Lys745Arg
NM_001346897.1:c.2099A>G NP_001333826.1:p.Lys700Arg
NM_001346898.1:c.2234A>G NP_001333827.1:p.Lys745Arg
NM_001346899.1:c.2099A>G NP_001333828.1:p.Lys700Arg
NM_001346900.1:c.2075A>G NP_001333829.1:p.Lys692Arg
NM_001346941.1:c.1433A>G NP_001333870.1:p.Lys478Arg
NM_005228.4:c.2234A>G NP_005219.2:p.Lys745Arg
NM_005228.5:c.2234A>G MANE Select NP_005219.2:p.Lys745Arg
NM_001346897.2:c.2099A>G NP_001333826.1:p.Lys700Arg
NM_001346898.2:c.2234A>G NP_001333827.1:p.Lys745Arg
NM_001346900.2:c.2075A>G NP_001333829.1:p.Lys692Arg
NM_001346941.2:c.1433A>G NP_001333870.1:p.Lys478Arg
NM_001346899.2:c.2099A>G NP_001333828.1:p.Lys700Arg