Canonical Allele Identifier: CA1708918316
Gene: EGFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174772_55174789delinsGGAATTAAGAGAAGCAAC , CM000669.2:g.55174772_55174789delinsGGAATTAAGAGAAGCAAC GRCh38
NC_000007.13:g.55242465_55242482delinsGGAATTAAGAGAAGCAAC , CM000669.1:g.55242465_55242482delinsGGAATTAAGAGAAGCAAC GRCh37
NC_000007.12:g.55209959_55209976delinsGGAATTAAGAGAAGCAAC NCBI36
NG_007726.3:g.160741_160758delinsGGAATTAAGAGAAGCAAC , LRG_304:g.160741_160758delinsGGAATTAAGAGAAGCAAC

Transcript Alleles

HGVS Amino-acid change
ENST00000275493.7:c.2235_2252delinsGGAATTAAGAGAAGCAAC MANE Select ENSP00000275493.2:p.Lys745=
ENST00000275493.6:c.2235_2252delinsGGAATTAAGAGAAGCAAC ENSP00000275493.2:p.Lys745=
ENST00000442591.5:c.*28+1844_*28+1861delinsGGAATTAAGAGAAGCAAC ENSP00000410031.1:p.=
ENST00000454757.6:c.2100_2117delinsGGAATTAAGAGAAGCAAC ENSP00000395243.3:p.Lys700=
ENST00000455089.5:c.2100_2117delinsGGAATTAAGAGAAGCAAC ENSP00000415559.1:p.Lys700=
NM_005228.3:c.2235_2252delinsGGAATTAAGAGAAGCAAC , LRG_304t1:c.2235_2252delinsGGAATTAAGAGAAGCAAC NP_005219.2:p.Lys745=
NM_001346897.1:c.2100_2117delinsGGAATTAAGAGAAGCAAC NP_001333826.1:p.Lys700=
NM_001346898.1:c.2235_2252delinsGGAATTAAGAGAAGCAAC NP_001333827.1:p.Lys745=
NM_001346899.1:c.2100_2117delinsGGAATTAAGAGAAGCAAC NP_001333828.1:p.Lys700=
NM_001346900.1:c.2076_2093delinsGGAATTAAGAGAAGCAAC NP_001333829.1:p.Lys692=
NM_001346941.1:c.1434_1451delinsGGAATTAAGAGAAGCAAC NP_001333870.1:p.Lys478=
NM_005228.4:c.2235_2252delinsGGAATTAAGAGAAGCAAC NP_005219.2:p.Lys745=
NM_005228.5:c.2235_2252delinsGGAATTAAGAGAAGCAAC MANE Select NP_005219.2:p.Lys745=
NM_001346897.2:c.2100_2117delinsGGAATTAAGAGAAGCAAC NP_001333826.1:p.Lys700=
NM_001346898.2:c.2235_2252delinsGGAATTAAGAGAAGCAAC NP_001333827.1:p.Lys745=
NM_001346900.2:c.2076_2093delinsGGAATTAAGAGAAGCAAC NP_001333829.1:p.Lys692=
NM_001346941.2:c.1434_1451delinsGGAATTAAGAGAAGCAAC NP_001333870.1:p.Lys478=
NM_001346899.2:c.2100_2117delinsGGAATTAAGAGAAGCAAC NP_001333828.1:p.Lys700=