Canonical Allele Identifier: CA1708918375

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174818G= , CM000669.2:g.55174818G=	GRCh38
NC_000007.13:g.55242511G= , CM000669.1:g.55242511G=	GRCh37
NC_000007.12:g.55210005G=	NCBI36
NG_007726.3:g.160787G= , LRG_304:g.160787G=

Transcript Alleles

HGVS	Amino-acid Change
NM_005228.5:c.2281G= MANE Select	NP_005219.2:p.Asp761=
ENST00000275493.7:c.2281G= MANE Select	ENSP00000275493.2:p.Asp761=
NM_001346897.1:c.2146G=	NP_001333826.1:p.Asp716=
NM_001346897.2:c.2146G=	NP_001333826.1:p.Asp716=
NM_001346898.1:c.2281G=	NP_001333827.1:p.Asp761=
NM_001346898.2:c.2281G=	NP_001333827.1:p.Asp761=
NM_001346899.1:c.2146G=	NP_001333828.1:p.Asp716=
NM_001346899.2:c.2146G=	NP_001333828.1:p.Asp716=
NM_001346900.1:c.2122G=	NP_001333829.1:p.Asp708=
NM_001346900.2:c.2122G=	NP_001333829.1:p.Asp708=
NM_001346941.1:c.1480G=	NP_001333870.1:p.Asp494=
NM_001346941.2:c.1480G=	NP_001333870.1:p.Asp494=
NM_005228.3:c.2281G= , LRG_304t1:c.2281G=	NP_005219.2:p.Asp761=
NM_005228.4:c.2281G=	NP_005219.2:p.Asp761=
ENST00000275493.6:c.2281G=	ENSP00000275493.2:p.Asp761=
ENST00000442591.5:c.*28+1890G=	ENSP00000410031.1:n.*28+1890G=
ENST00000450046.2:c.2122G=	ENSP00000413354.2:p.Asp708=
ENST00000454757.6:c.2146G=	ENSP00000395243.3:p.Asp716=
ENST00000455089.5:c.2146G=	ENSP00000415559.1:p.Asp716=
ENST00000700145.1:c.630G=