Canonical Allele Identifier: CA891842001
Gene: EGFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174774_55174785del , CM000669.2:g.55174774_55174785del GRCh38
NC_000007.13:g.55242467_55242478del , CM000669.1:g.55242467_55242478del GRCh37
NC_000007.12:g.55209961_55209972del NCBI36
NG_007726.3:g.160743_160754del , LRG_304:g.160743_160754del

Transcript Alleles

HGVS Amino-acid change
ENST00000275493.7:c.2237_2248del MANE Select ENSP00000275493.2:p.Glu746_Glu749del
ENST00000275493.6:c.2237_2248del ENSP00000275493.2:p.Glu746_Glu749del
ENST00000442591.5:c.*28+1846_*28+1857del ENSP00000410031.1:p.=
ENST00000454757.6:c.2102_2113del ENSP00000395243.3:p.Glu701_Glu704del
ENST00000455089.5:c.2102_2113del ENSP00000415559.1:p.Glu701_Glu704del
NM_005228.3:c.2237_2248del , LRG_304t1:c.2237_2248del NP_005219.2:p.Glu746_Glu749del
NM_001346897.1:c.2102_2113del NP_001333826.1:p.Glu701_Glu704del
NM_001346898.1:c.2237_2248del NP_001333827.1:p.Glu746_Glu749del
NM_001346899.1:c.2102_2113del NP_001333828.1:p.Glu701_Glu704del
NM_001346900.1:c.2078_2089del NP_001333829.1:p.Glu693_Glu696del
NM_001346941.1:c.1436_1447del NP_001333870.1:p.Glu479_Glu482del
NM_005228.4:c.2237_2248del NP_005219.2:p.Glu746_Glu749del
NM_005228.5:c.2237_2248del MANE Select NP_005219.2:p.Glu746_Glu749del
NM_001346897.2:c.2102_2113del NP_001333826.1:p.Glu701_Glu704del
NM_001346898.2:c.2237_2248del NP_001333827.1:p.Glu746_Glu749del
NM_001346900.2:c.2078_2089del NP_001333829.1:p.Glu693_Glu696del
NM_001346941.2:c.1436_1447del NP_001333870.1:p.Glu479_Glu482del
NM_001346899.2:c.2102_2113del NP_001333828.1:p.Glu701_Glu704del