Canonical Allele Identifier: CA1708918307
Gene: EGFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174768T= , CM000669.2:g.55174768T= GRCh38
NC_000007.13:g.55242461T= , CM000669.1:g.55242461T= GRCh37
NC_000007.12:g.55209955T= NCBI36
NG_007726.3:g.160737T= , LRG_304:g.160737T=

Transcript Alleles

HGVS Amino-acid change
ENST00000275493.7:c.2231T= MANE Select ENSP00000275493.2:p.Ile744=
ENST00000275493.6:c.2231T= ENSP00000275493.2:p.Ile744=
ENST00000442591.5:c.*28+1840T= ENSP00000410031.1:n.*28+1840T=
ENST00000454757.6:c.2096T= ENSP00000395243.3:p.Ile699=
ENST00000455089.5:c.2096T= ENSP00000415559.1:p.Ile699=
NM_005228.3:c.2231T= , LRG_304t1:c.2231T= NP_005219.2:p.Ile744=
NM_001346897.1:c.2096T= NP_001333826.1:p.Ile699=
NM_001346898.1:c.2231T= NP_001333827.1:p.Ile744=
NM_001346899.1:c.2096T= NP_001333828.1:p.Ile699=
NM_001346900.1:c.2072T= NP_001333829.1:p.Ile691=
NM_001346941.1:c.1430T= NP_001333870.1:p.Ile477=
NM_005228.4:c.2231T= NP_005219.2:p.Ile744=
NM_005228.5:c.2231T= MANE Select NP_005219.2:p.Ile744=
NM_001346897.2:c.2096T= NP_001333826.1:p.Ile699=
NM_001346898.2:c.2231T= NP_001333827.1:p.Ile744=
NM_001346900.2:c.2072T= NP_001333829.1:p.Ile691=
NM_001346941.2:c.1430T= NP_001333870.1:p.Ile477=
NM_001346899.2:c.2096T= NP_001333828.1:p.Ile699=