Canonical Allele Identifier: CA1708922648
Gene: EGFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55191825C= , CM000669.2:g.55191825C= GRCh38
NC_000007.13:g.55259518C= , CM000669.1:g.55259518C= GRCh37
NC_000007.12:g.55227012C= NCBI36
NG_007726.3:g.177794C= , LRG_304:g.177794C=

Transcript Alleles

HGVS Amino-acid change
ENST00000275493.7:c.2576C= MANE Select ENSP00000275493.2:p.Ala859=
ENST00000275493.6:c.2576C= ENSP00000275493.2:p.Ala859=
ENST00000442591.5:c.*28+18897C= ENSP00000410031.1:n.*28+18897C=
ENST00000454757.6:c.2441C= ENSP00000395243.3:p.Ala814=
ENST00000455089.5:c.2441C= ENSP00000415559.1:p.Ala814=
NM_005228.3:c.2576C= , LRG_304t1:c.2576C= NP_005219.2:p.Ala859=
NM_001346897.1:c.2441C= NP_001333826.1:p.Ala814=
NM_001346898.1:c.2576C= NP_001333827.1:p.Ala859=
NM_001346899.1:c.2441C= NP_001333828.1:p.Ala814=
NM_001346900.1:c.2417C= NP_001333829.1:p.Ala806=
NM_001346941.1:c.1775C= NP_001333870.1:p.Ala592=
NM_005228.4:c.2576C= NP_005219.2:p.Ala859=
NM_005228.5:c.2576C= MANE Select NP_005219.2:p.Ala859=
NM_001346897.2:c.2441C= NP_001333826.1:p.Ala814=
NM_001346898.2:c.2576C= NP_001333827.1:p.Ala859=
NM_001346900.2:c.2417C= NP_001333829.1:p.Ala806=
NM_001346941.2:c.1775C= NP_001333870.1:p.Ala592=
NM_001346899.2:c.2441C= NP_001333828.1:p.Ala814=