Canonical Allele Identifier: CA645561487
Gene: EGFR HGNC NCBI

Linked Data

COSMIC: COSM28517

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174772_55174783del , CM000669.2:g.55174772_55174783del GRCh38
NC_000007.13:g.55242465_55242476del , CM000669.1:g.55242465_55242476del GRCh37
NC_000007.12:g.55209959_55209970del NCBI36
NG_007726.3:g.160741_160752del , LRG_304:g.160741_160752del

Transcript Alleles

HGVS Amino-acid change
ENST00000275493.7:c.2235_2246del MANE Select ENSP00000275493.2:p.Glu746_Glu749del
ENST00000275493.6:c.2235_2246del ENSP00000275493.2:p.Glu746_Glu749del
ENST00000442591.5:c.*28+1844_*28+1855del ENSP00000410031.1:p.=
ENST00000454757.6:c.2100_2111del ENSP00000395243.3:p.Glu701_Glu704del
ENST00000455089.5:c.2100_2111del ENSP00000415559.1:p.Glu701_Glu704del
NM_005228.3:c.2235_2246del , LRG_304t1:c.2235_2246del NP_005219.2:p.Glu746_Glu749del
NM_001346897.1:c.2100_2111del NP_001333826.1:p.Glu701_Glu704del
NM_001346898.1:c.2235_2246del NP_001333827.1:p.Glu746_Glu749del
NM_001346899.1:c.2100_2111del NP_001333828.1:p.Glu701_Glu704del
NM_001346900.1:c.2076_2087del NP_001333829.1:p.Glu693_Glu696del
NM_001346941.1:c.1434_1445del NP_001333870.1:p.Glu479_Glu482del
NM_005228.4:c.2235_2246del NP_005219.2:p.Glu746_Glu749del
NM_005228.5:c.2235_2246del MANE Select NP_005219.2:p.Glu746_Glu749del
NM_001346897.2:c.2100_2111del NP_001333826.1:p.Glu701_Glu704del
NM_001346898.2:c.2235_2246del NP_001333827.1:p.Glu746_Glu749del
NM_001346900.2:c.2076_2087del NP_001333829.1:p.Glu693_Glu696del
NM_001346941.2:c.1434_1445del NP_001333870.1:p.Glu479_Glu482del
NM_001346899.2:c.2100_2111del NP_001333828.1:p.Glu701_Glu704del