Canonical Allele Identifier: CA1708922644

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55191824_55191825delinsGC , CM000669.2:g.55191824_55191825delinsGC	GRCh38
NC_000007.13:g.55259517_55259518delinsGC , CM000669.1:g.55259517_55259518delinsGC	GRCh37
NC_000007.12:g.55227011_55227012delinsGC	NCBI36
NG_007726.3:g.177793_177794delinsGC , LRG_304:g.177793_177794delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2416_2417delinsGC	ENSP00000413354.2:p.Ala806=
ENST00000700145.1:c.899+25_899+26delinsGC
ENST00000275493.7:c.2575_2576delinsGC MANE Select	ENSP00000275493.2:p.Ala859=
ENST00000275493.6:c.2575_2576delinsGC	ENSP00000275493.2:p.Ala859=
ENST00000442591.5:c.*28+18896_*28+18897delinsGC	ENSP00000410031.1:n.*28+18896_*28+18897de...
ENST00000454757.6:c.2440_2441delinsGC	ENSP00000395243.3:p.Ala814=
ENST00000455089.5:c.2440_2441delinsGC	ENSP00000415559.1:p.Ala814=
NM_005228.3:c.2575_2576delinsGC , LRG_304t1:c.2575_2576delinsGC	NP_005219.2:p.Ala859=
NM_001346897.1:c.2440_2441delinsGC	NP_001333826.1:p.Ala814=
NM_001346898.1:c.2575_2576delinsGC	NP_001333827.1:p.Ala859=
NM_001346899.1:c.2440_2441delinsGC	NP_001333828.1:p.Ala814=
NM_001346900.1:c.2416_2417delinsGC	NP_001333829.1:p.Ala806=
NM_001346941.1:c.1774_1775delinsGC	NP_001333870.1:p.Ala592=
NM_005228.4:c.2575_2576delinsGC	NP_005219.2:p.Ala859=
NM_005228.5:c.2575_2576delinsGC MANE Select	NP_005219.2:p.Ala859=
NM_001346897.2:c.2440_2441delinsGC	NP_001333826.1:p.Ala814=
NM_001346898.2:c.2575_2576delinsGC	NP_001333827.1:p.Ala859=
NM_001346900.2:c.2416_2417delinsGC	NP_001333829.1:p.Ala806=
NM_001346941.2:c.1774_1775delinsGC	NP_001333870.1:p.Ala592=
NM_001346899.2:c.2440_2441delinsGC	NP_001333828.1:p.Ala814=