Canonical Allele Identifier: CA3250100690

Gene: EGFR

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_005228.5:c.2236delinsCAATCTC MANE Select	NP_005219.2:p.Glu746delinsGlnSerGln
ENST00000275493.7:c.2236delinsCAATCTC MANE Select	ENSP00000275493.2:p.Glu746delinsGlnSerGln
NM_001346897.1:c.2101delinsCAATCTC	NP_001333826.1:p.Glu701delinsGlnSerGln
NM_001346897.2:c.2101delinsCAATCTC	NP_001333826.1:p.Glu701delinsGlnSerGln
NM_001346898.1:c.2236delinsCAATCTC	NP_001333827.1:p.Glu746delinsGlnSerGln
NM_001346898.2:c.2236delinsCAATCTC	NP_001333827.1:p.Glu746delinsGlnSerGln
NM_001346899.1:c.2101delinsCAATCTC	NP_001333828.1:p.Glu701delinsGlnSerGln
NM_001346899.2:c.2101delinsCAATCTC	NP_001333828.1:p.Glu701delinsGlnSerGln
NM_001346900.1:c.2077delinsCAATCTC	NP_001333829.1:p.Glu693delinsGlnSerGln
NM_001346900.2:c.2077delinsCAATCTC	NP_001333829.1:p.Glu693delinsGlnSerGln
NM_001346941.1:c.1435delinsCAATCTC	NP_001333870.1:p.Glu479delinsGlnSerGln
NM_001346941.2:c.1435delinsCAATCTC	NP_001333870.1:p.Glu479delinsGlnSerGln
NM_005228.3:c.2236delinsCAATCTC , LRG_304t1:c.2236delinsCAATCTC	NP_005219.2:p.Glu746delinsGlnSerGln
NM_005228.4:c.2236delinsCAATCTC	NP_005219.2:p.Glu746delinsGlnSerGln
ENST00000275493.6:c.2236delinsCAATCTC	ENSP00000275493.2:p.Glu746delinsGlnSerGln
ENST00000442591.5:c.*28+1845delinsCAATCTC	ENSP00000410031.1:n.*28+1845delinsCAATCTC
ENST00000450046.2:c.2077delinsCAATCTC	ENSP00000413354.2:p.Glu693delinsGlnSerGln
ENST00000454757.6:c.2101delinsCAATCTC	ENSP00000395243.3:p.Glu701delinsGlnSerGln
ENST00000455089.5:c.2101delinsCAATCTC	ENSP00000415559.1:p.Glu701delinsGlnSerGln
ENST00000700145.1:c.585delinsCAATCTC