Canonical Allele Identifier: CA367584003
Gene: EGFR HGNC NCBI

Linked Data

COSMIC: COSM329081

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174738A>G , CM000669.2:g.55174738A>G GRCh38
NC_000007.13:g.55242431A>G , CM000669.1:g.55242431A>G GRCh37
NC_000007.12:g.55209925A>G NCBI36
NG_007726.3:g.160707A>G , LRG_304:g.160707A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2042A>G ENSP00000413354.2:p.Glu681Gly
ENST00000700145.1:c.550A>G
ENST00000275493.7:c.2201A>G MANE Select ENSP00000275493.2:p.Glu734Gly
ENST00000275493.6:c.2201A>G ENSP00000275493.2:p.Glu734Gly
ENST00000442591.5:c.*28+1810A>G ENSP00000410031.1:n.*28+1810A>G
ENST00000454757.6:c.2066A>G ENSP00000395243.3:p.Glu689Gly
ENST00000455089.5:c.2066A>G ENSP00000415559.1:p.Glu689Gly
NM_005228.3:c.2201A>G , LRG_304t1:c.2201A>G NP_005219.2:p.Glu734Gly
NM_001346897.1:c.2066A>G NP_001333826.1:p.Glu689Gly
NM_001346898.1:c.2201A>G NP_001333827.1:p.Glu734Gly
NM_001346899.1:c.2066A>G NP_001333828.1:p.Glu689Gly
NM_001346900.1:c.2042A>G NP_001333829.1:p.Glu681Gly
NM_001346941.1:c.1400A>G NP_001333870.1:p.Glu467Gly
NM_005228.4:c.2201A>G NP_005219.2:p.Glu734Gly
NM_005228.5:c.2201A>G MANE Select NP_005219.2:p.Glu734Gly
NM_001346897.2:c.2066A>G NP_001333826.1:p.Glu689Gly
NM_001346898.2:c.2201A>G NP_001333827.1:p.Glu734Gly
NM_001346900.2:c.2042A>G NP_001333829.1:p.Glu681Gly
NM_001346941.2:c.1400A>G NP_001333870.1:p.Glu467Gly
NM_001346899.2:c.2066A>G NP_001333828.1:p.Glu689Gly