Canonical Allele Identifier: CA1708922531
Gene: EGFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55191772G= , CM000669.2:g.55191772G= GRCh38
NC_000007.13:g.55259465G= , CM000669.1:g.55259465G= GRCh37
NC_000007.12:g.55226959G= NCBI36
NG_007726.3:g.177741G= , LRG_304:g.177741G=

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2364G= ENSP00000413354.2:p.Arg788=
ENST00000700145.1:c.872G=
ENST00000275493.7:c.2523G= MANE Select ENSP00000275493.2:p.Arg841=
ENST00000275493.6:c.2523G= ENSP00000275493.2:p.Arg841=
ENST00000442591.5:c.*28+18844G= ENSP00000410031.1:n.*28+18844G=
ENST00000454757.6:c.2388G= ENSP00000395243.3:p.Arg796=
ENST00000455089.5:c.2388G= ENSP00000415559.1:p.Arg796=
NM_005228.3:c.2523G= , LRG_304t1:c.2523G= NP_005219.2:p.Arg841=
NM_001346897.1:c.2388G= NP_001333826.1:p.Arg796=
NM_001346898.1:c.2523G= NP_001333827.1:p.Arg841=
NM_001346899.1:c.2388G= NP_001333828.1:p.Arg796=
NM_001346900.1:c.2364G= NP_001333829.1:p.Arg788=
NM_001346941.1:c.1722G= NP_001333870.1:p.Arg574=
NM_005228.4:c.2523G= NP_005219.2:p.Arg841=
NM_005228.5:c.2523G= MANE Select NP_005219.2:p.Arg841=
NM_001346897.2:c.2388G= NP_001333826.1:p.Arg796=
NM_001346898.2:c.2523G= NP_001333827.1:p.Arg841=
NM_001346900.2:c.2364G= NP_001333829.1:p.Arg788=
NM_001346941.2:c.1722G= NP_001333870.1:p.Arg574=
NM_001346899.2:c.2388G= NP_001333828.1:p.Arg796=