Canonical Allele Identifier: CA2850447141

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174769_55174786delinsTAAG , CM000669.2:g.55174769_55174786delinsTAAG	GRCh38
NC_000007.13:g.55242462_55242479delinsTAAG , CM000669.1:g.55242462_55242479delinsTAAG	GRCh37
NC_000007.12:g.55209956_55209973delinsTAAG	NCBI36
NG_007726.3:g.160738_160755delinsTAAG , LRG_304:g.160738_160755delinsTAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2073_2090delinsTAAG	ENSP00000413354.2:p.Glu693AsnfsTer12
ENST00000700145.1:c.581_598delinsTAAG
ENST00000275493.7:c.2232_2249delinsTAAG MANE Select	ENSP00000275493.2:p.Glu746AsnfsTer12
ENST00000275493.6:c.2232_2249delinsTAAG	ENSP00000275493.2:p.Glu746AsnfsTer12
ENST00000442591.5:c.*28+1841_*28+1858delinsTAAG	ENSP00000410031.1:n.*28+1841_*28+1858delinsTAAG
ENST00000454757.6:c.2097_2114delinsTAAG	ENSP00000395243.3:p.Glu701AsnfsTer12
ENST00000455089.5:c.2097_2114delinsTAAG	ENSP00000415559.1:p.Glu701AsnfsTer12
NM_005228.3:c.2232_2249delinsTAAG , LRG_304t1:c.2232_2249delinsTAAG	NP_005219.2:p.Glu746AsnfsTer12
NM_001346897.1:c.2097_2114delinsTAAG	NP_001333826.1:p.Glu701AsnfsTer12
NM_001346898.1:c.2232_2249delinsTAAG	NP_001333827.1:p.Glu746AsnfsTer12
NM_001346899.1:c.2097_2114delinsTAAG	NP_001333828.1:p.Glu701AsnfsTer12
NM_001346900.1:c.2073_2090delinsTAAG	NP_001333829.1:p.Glu693AsnfsTer12
NM_001346941.1:c.1431_1448delinsTAAG	NP_001333870.1:p.Glu479AsnfsTer12
NM_005228.4:c.2232_2249delinsTAAG	NP_005219.2:p.Glu746AsnfsTer12
NM_005228.5:c.2232_2249delinsTAAG MANE Select	NP_005219.2:p.Glu746AsnfsTer12
NM_001346897.2:c.2097_2114delinsTAAG	NP_001333826.1:p.Glu701AsnfsTer12
NM_001346898.2:c.2232_2249delinsTAAG	NP_001333827.1:p.Glu746AsnfsTer12
NM_001346900.2:c.2073_2090delinsTAAG	NP_001333829.1:p.Glu693AsnfsTer12
NM_001346941.2:c.1431_1448delinsTAAG	NP_001333870.1:p.Glu479AsnfsTer12
NM_001346899.2:c.2097_2114delinsTAAG	NP_001333828.1:p.Glu701AsnfsTer12