Canonical Allele Identifier: CA645561536
Gene: EGFR HGNC NCBI

Linked Data

COSMIC: COSM26439

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174785_55174811del , CM000669.2:g.55174785_55174811del GRCh38
NC_000007.13:g.55242478_55242504del , CM000669.1:g.55242478_55242504del GRCh37
NC_000007.12:g.55209972_55209998del NCBI36
NG_007726.3:g.160754_160780del , LRG_304:g.160754_160780del

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2089_2115del ENSP00000413354.2:p.Ala697_Glu705del
ENST00000700145.1:c.597_623del
ENST00000275493.7:c.2248_2274del MANE Select ENSP00000275493.2:p.Ala750_Glu758del
ENST00000275493.6:c.2248_2274del ENSP00000275493.2:p.Ala750_Glu758del
ENST00000442591.5:c.*28+1857_*28+1883del ENSP00000410031.1:n.*28+1857_*28+1883del
ENST00000454757.6:c.2113_2139del ENSP00000395243.3:p.Ala705_Glu713del
ENST00000455089.5:c.2113_2139del ENSP00000415559.1:p.Ala705_Glu713del
NM_005228.3:c.2248_2274del , LRG_304t1:c.2248_2274del NP_005219.2:p.Ala750_Glu758del
NM_001346897.1:c.2113_2139del NP_001333826.1:p.Ala705_Glu713del
NM_001346898.1:c.2248_2274del NP_001333827.1:p.Ala750_Glu758del
NM_001346899.1:c.2113_2139del NP_001333828.1:p.Ala705_Glu713del
NM_001346900.1:c.2089_2115del NP_001333829.1:p.Ala697_Glu705del
NM_001346941.1:c.1447_1473del NP_001333870.1:p.Ala483_Glu491del
NM_005228.4:c.2248_2274del NP_005219.2:p.Ala750_Glu758del
NM_005228.5:c.2248_2274del MANE Select NP_005219.2:p.Ala750_Glu758del
NM_001346897.2:c.2113_2139del NP_001333826.1:p.Ala705_Glu713del
NM_001346898.2:c.2248_2274del NP_001333827.1:p.Ala750_Glu758del
NM_001346900.2:c.2089_2115del NP_001333829.1:p.Ala697_Glu705del
NM_001346941.2:c.1447_1473del NP_001333870.1:p.Ala483_Glu491del
NM_001346899.2:c.2113_2139del NP_001333828.1:p.Ala705_Glu713del