Canonical Allele Identifier: CA2850447142

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174769_55174787delinsTAAG , CM000669.2:g.55174769_55174787delinsTAAG	GRCh38
NC_000007.13:g.55242462_55242480delinsTAAG , CM000669.1:g.55242462_55242480delinsTAAG	GRCh37
NC_000007.12:g.55209956_55209974delinsTAAG	NCBI36
NG_007726.3:g.160738_160756delinsTAAG , LRG_304:g.160738_160756delinsTAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2073_2091delinsTAAG	ENSP00000413354.2:p.Glu693_Ala697del
ENST00000700145.1:c.581_599delinsTAAG
ENST00000275493.7:c.2232_2250delinsTAAG MANE Select	ENSP00000275493.2:p.Glu746_Ala750del
ENST00000275493.6:c.2232_2250delinsTAAG	ENSP00000275493.2:p.Glu746_Ala750del
ENST00000442591.5:c.*28+1841_*28+1859delinsTAAG	ENSP00000410031.1:n.*28+1841_*28+1859delinsTAAG
ENST00000454757.6:c.2097_2115delinsTAAG	ENSP00000395243.3:p.Glu701_Ala705del
ENST00000455089.5:c.2097_2115delinsTAAG	ENSP00000415559.1:p.Glu701_Ala705del
NM_005228.3:c.2232_2250delinsTAAG , LRG_304t1:c.2232_2250delinsTAAG	NP_005219.2:p.Glu746_Ala750del
NM_001346897.1:c.2097_2115delinsTAAG	NP_001333826.1:p.Glu701_Ala705del
NM_001346898.1:c.2232_2250delinsTAAG	NP_001333827.1:p.Glu746_Ala750del
NM_001346899.1:c.2097_2115delinsTAAG	NP_001333828.1:p.Glu701_Ala705del
NM_001346900.1:c.2073_2091delinsTAAG	NP_001333829.1:p.Glu693_Ala697del
NM_001346941.1:c.1431_1449delinsTAAG	NP_001333870.1:p.Glu479_Ala483del
NM_005228.4:c.2232_2250delinsTAAG	NP_005219.2:p.Glu746_Ala750del
NM_005228.5:c.2232_2250delinsTAAG MANE Select	NP_005219.2:p.Glu746_Ala750del
NM_001346897.2:c.2097_2115delinsTAAG	NP_001333826.1:p.Glu701_Ala705del
NM_001346898.2:c.2232_2250delinsTAAG	NP_001333827.1:p.Glu746_Ala750del
NM_001346900.2:c.2073_2091delinsTAAG	NP_001333829.1:p.Glu693_Ala697del
NM_001346941.2:c.1431_1449delinsTAAG	NP_001333870.1:p.Glu479_Ala483del
NM_001346899.2:c.2097_2115delinsTAAG	NP_001333828.1:p.Glu701_Ala705del