Canonical Allele Identifier: CA367580135
Gene: EGFR HGNC NCBI

Linked Data

dbSNP Id: rs2128964450

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55191754C>A , CM000669.2:g.55191754C>A GRCh38
NC_000007.13:g.55259447C>A , CM000669.1:g.55259447C>A GRCh37
NC_000007.12:g.55226941C>A NCBI36
NG_007726.3:g.177723C>A , LRG_304:g.177723C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2346C>A ENSP00000413354.2:p.His782Gln
ENST00000700145.1:c.854C>A
ENST00000275493.7:c.2505C>A MANE Select ENSP00000275493.2:p.His835Gln
ENST00000275493.6:c.2505C>A ENSP00000275493.2:p.His835Gln
ENST00000442591.5:c.*28+18826C>A ENSP00000410031.1:n.*28+18826C>A
ENST00000454757.6:c.2370C>A ENSP00000395243.3:p.His790Gln
ENST00000455089.5:c.2370C>A ENSP00000415559.1:p.His790Gln
NM_005228.3:c.2505C>A , LRG_304t1:c.2505C>A NP_005219.2:p.His835Gln
NM_001346897.1:c.2370C>A NP_001333826.1:p.His790Gln
NM_001346898.1:c.2505C>A NP_001333827.1:p.His835Gln
NM_001346899.1:c.2370C>A NP_001333828.1:p.His790Gln
NM_001346900.1:c.2346C>A NP_001333829.1:p.His782Gln
NM_001346941.1:c.1704C>A NP_001333870.1:p.His568Gln
NM_005228.4:c.2505C>A NP_005219.2:p.His835Gln
NM_005228.5:c.2505C>A MANE Select NP_005219.2:p.His835Gln
NM_001346897.2:c.2370C>A NP_001333826.1:p.His790Gln
NM_001346898.2:c.2505C>A NP_001333827.1:p.His835Gln
NM_001346900.2:c.2346C>A NP_001333829.1:p.His782Gln
NM_001346941.2:c.1704C>A NP_001333870.1:p.His568Gln
NM_001346899.2:c.2370C>A NP_001333828.1:p.His790Gln