Canonical Allele Identifier: CA1708922644
Gene: EGFR HGNC NCBI

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
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=