Canonical Allele Identifier: CA645561614
Gene: EGFR HGNC NCBI

Linked Data

COSMIC: COSM26351

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000275493.7:c.2575dup MANE Select ENSP00000275493.2:p.Ala859GlyfsTer?
ENST00000275493.6:c.2575dup ENSP00000275493.2:p.Ala859GlyfsTer?
ENST00000442591.5:c.*28+18896dup ENSP00000410031.1:n.*28+18896dup
ENST00000454757.6:c.2440dup ENSP00000395243.3:p.Ala814GlyfsTer?
ENST00000455089.5:c.2440dup ENSP00000415559.1:p.Ala814GlyfsTer?
NM_005228.3:c.2575dup , LRG_304t1:c.2575dup NP_005219.2:p.Ala859GlyfsTer?
NM_001346897.1:c.2440dup NP_001333826.1:p.Ala814GlyfsTer?
NM_001346898.1:c.2575dup NP_001333827.1:p.Ala859GlyfsTer?
NM_001346899.1:c.2440dup NP_001333828.1:p.Ala814GlyfsTer?
NM_001346900.1:c.2416dup NP_001333829.1:p.Ala806GlyfsTer?
NM_001346941.1:c.1774dup NP_001333870.1:p.Ala592GlyfsTer?
NM_005228.4:c.2575dup NP_005219.2:p.Ala859GlyfsTer?
NM_005228.5:c.2575dup MANE Select NP_005219.2:p.Ala859GlyfsTer?
NM_001346897.2:c.2440dup NP_001333826.1:p.Ala814GlyfsTer?
NM_001346898.2:c.2575dup NP_001333827.1:p.Ala859GlyfsTer?
NM_001346900.2:c.2416dup NP_001333829.1:p.Ala806GlyfsTer?
NM_001346941.2:c.1774dup NP_001333870.1:p.Ala592GlyfsTer?
NM_001346899.2:c.2440dup NP_001333828.1:p.Ala814GlyfsTer?