Canonical Allele Identifier: CA645561543

Gene: EGFR

Linked Data

• COSMIC: COSM23634 ; COSM133207

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174789_55174812del , CM000669.2:g.55174789_55174812del	GRCh38
NC_000007.13:g.55242482_55242505del , CM000669.1:g.55242482_55242505del	GRCh37
NC_000007.12:g.55209976_55209999del	NCBI36
NG_007726.3:g.160758_160781del , LRG_304:g.160758_160781del

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2093_2116del	ENSP00000413354.2:p.Thr698_Glu705del
ENST00000700145.1:c.601_624del
ENST00000275493.7:c.2252_2275del MANE Select	ENSP00000275493.2:p.Thr751_Glu758del
ENST00000275493.6:c.2252_2275del	ENSP00000275493.2:p.Thr751_Glu758del
ENST00000442591.5:c.*28+1861_*28+1884del	ENSP00000410031.1:n.*28+1861_*28+1884del
ENST00000454757.6:c.2117_2140del	ENSP00000395243.3:p.Thr706_Glu713del
ENST00000455089.5:c.2117_2140del	ENSP00000415559.1:p.Thr706_Glu713del
NM_005228.3:c.2252_2275del , LRG_304t1:c.2252_2275del	NP_005219.2:p.Thr751_Glu758del
NM_001346897.1:c.2117_2140del	NP_001333826.1:p.Thr706_Glu713del
NM_001346898.1:c.2252_2275del	NP_001333827.1:p.Thr751_Glu758del
NM_001346899.1:c.2117_2140del	NP_001333828.1:p.Thr706_Glu713del
NM_001346900.1:c.2093_2116del	NP_001333829.1:p.Thr698_Glu705del
NM_001346941.1:c.1451_1474del	NP_001333870.1:p.Thr484_Glu491del
NM_005228.4:c.2252_2275del	NP_005219.2:p.Thr751_Glu758del
NM_005228.5:c.2252_2275del MANE Select	NP_005219.2:p.Thr751_Glu758del
NM_001346897.2:c.2117_2140del	NP_001333826.1:p.Thr706_Glu713del
NM_001346898.2:c.2252_2275del	NP_001333827.1:p.Thr751_Glu758del
NM_001346900.2:c.2093_2116del	NP_001333829.1:p.Thr698_Glu705del
NM_001346941.2:c.1451_1474del	NP_001333870.1:p.Thr484_Glu491del
NM_001346899.2:c.2117_2140del	NP_001333828.1:p.Thr706_Glu713del