Canonical Allele Identifier: CA367583982
Gene: EGFR HGNC NCBI

Linked Data

dbSNP Id: rs2128954588

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174733C>G , CM000669.2:g.55174733C>G GRCh38
NC_000007.13:g.55242426C>G , CM000669.1:g.55242426C>G GRCh37
NC_000007.12:g.55209920C>G NCBI36
NG_007726.3:g.160702C>G , LRG_304:g.160702C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2037C>G ENSP00000413354.2:p.Ile679Met
ENST00000700145.1:c.545C>G
ENST00000275493.7:c.2196C>G MANE Select ENSP00000275493.2:p.Ile732Met
ENST00000275493.6:c.2196C>G ENSP00000275493.2:p.Ile732Met
ENST00000442591.5:c.*28+1805C>G ENSP00000410031.1:n.*28+1805C>G
ENST00000454757.6:c.2061C>G ENSP00000395243.3:p.Ile687Met
ENST00000455089.5:c.2061C>G ENSP00000415559.1:p.Ile687Met
NM_005228.3:c.2196C>G , LRG_304t1:c.2196C>G NP_005219.2:p.Ile732Met
NM_001346897.1:c.2061C>G NP_001333826.1:p.Ile687Met
NM_001346898.1:c.2196C>G NP_001333827.1:p.Ile732Met
NM_001346899.1:c.2061C>G NP_001333828.1:p.Ile687Met
NM_001346900.1:c.2037C>G NP_001333829.1:p.Ile679Met
NM_001346941.1:c.1395C>G NP_001333870.1:p.Ile465Met
NM_005228.4:c.2196C>G NP_005219.2:p.Ile732Met
NM_005228.5:c.2196C>G MANE Select NP_005219.2:p.Ile732Met
NM_001346897.2:c.2061C>G NP_001333826.1:p.Ile687Met
NM_001346898.2:c.2196C>G NP_001333827.1:p.Ile732Met
NM_001346900.2:c.2037C>G NP_001333829.1:p.Ile679Met
NM_001346941.2:c.1395C>G NP_001333870.1:p.Ile465Met
NM_001346899.2:c.2061C>G NP_001333828.1:p.Ile687Met