Canonical Allele Identifier: CA3250100687

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174773delinsATTC , CM000669.2:g.55174773delinsATTC	GRCh38
NC_000007.13:g.55242466delinsATTC , CM000669.1:g.55242466delinsATTC	GRCh37
NC_000007.12:g.55209960delinsATTC	NCBI36
NG_007726.3:g.160742delinsATTC , LRG_304:g.160742delinsATTC

Transcript Alleles

HGVS	Amino-acid Change
NM_005228.5:c.2236delinsATTC MANE Select	NP_005219.2:p.Glu746delinsIleGln
ENST00000275493.7:c.2236delinsATTC MANE Select	ENSP00000275493.2:p.Glu746delinsIleGln
NM_001346897.1:c.2101delinsATTC	NP_001333826.1:p.Glu701delinsIleGln
NM_001346897.2:c.2101delinsATTC	NP_001333826.1:p.Glu701delinsIleGln
NM_001346898.1:c.2236delinsATTC	NP_001333827.1:p.Glu746delinsIleGln
NM_001346898.2:c.2236delinsATTC	NP_001333827.1:p.Glu746delinsIleGln
NM_001346899.1:c.2101delinsATTC	NP_001333828.1:p.Glu701delinsIleGln
NM_001346899.2:c.2101delinsATTC	NP_001333828.1:p.Glu701delinsIleGln
NM_001346900.1:c.2077delinsATTC	NP_001333829.1:p.Glu693delinsIleGln
NM_001346900.2:c.2077delinsATTC	NP_001333829.1:p.Glu693delinsIleGln
NM_001346941.1:c.1435delinsATTC	NP_001333870.1:p.Glu479delinsIleGln
NM_001346941.2:c.1435delinsATTC	NP_001333870.1:p.Glu479delinsIleGln
NM_005228.3:c.2236delinsATTC , LRG_304t1:c.2236delinsATTC	NP_005219.2:p.Glu746delinsIleGln
NM_005228.4:c.2236delinsATTC	NP_005219.2:p.Glu746delinsIleGln
ENST00000275493.6:c.2236delinsATTC	ENSP00000275493.2:p.Glu746delinsIleGln
ENST00000442591.5:c.*28+1845delinsATTC	ENSP00000410031.1:n.*28+1845delinsATTC
ENST00000450046.2:c.2077delinsATTC	ENSP00000413354.2:p.Glu693delinsIleGln
ENST00000454757.6:c.2101delinsATTC	ENSP00000395243.3:p.Glu701delinsIleGln
ENST00000455089.5:c.2101delinsATTC	ENSP00000415559.1:p.Glu701delinsIleGln
ENST00000700145.1:c.585delinsATTC