Canonical Allele Identifier: CA1708918367

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174805C= , CM000669.2:g.55174805C=	GRCh38
NC_000007.13:g.55242498C= , CM000669.1:g.55242498C=	GRCh37
NC_000007.12:g.55209992C=	NCBI36
NG_007726.3:g.160774C= , LRG_304:g.160774C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2109C=	ENSP00000413354.2:p.Asn703=
ENST00000700145.1:c.617C=
ENST00000275493.7:c.2268C= MANE Select	ENSP00000275493.2:p.Asn756=
ENST00000275493.6:c.2268C=	ENSP00000275493.2:p.Asn756=
ENST00000442591.5:c.*28+1877C=	ENSP00000410031.1:n.*28+1877C=
ENST00000454757.6:c.2133C=	ENSP00000395243.3:p.Asn711=
ENST00000455089.5:c.2133C=	ENSP00000415559.1:p.Asn711=
NM_005228.3:c.2268C= , LRG_304t1:c.2268C=	NP_005219.2:p.Asn756=
NM_001346897.1:c.2133C=	NP_001333826.1:p.Asn711=
NM_001346898.1:c.2268C=	NP_001333827.1:p.Asn756=
NM_001346899.1:c.2133C=	NP_001333828.1:p.Asn711=
NM_001346900.1:c.2109C=	NP_001333829.1:p.Asn703=
NM_001346941.1:c.1467C=	NP_001333870.1:p.Asn489=
NM_005228.4:c.2268C=	NP_005219.2:p.Asn756=
NM_005228.5:c.2268C= MANE Select	NP_005219.2:p.Asn756=
NM_001346897.2:c.2133C=	NP_001333826.1:p.Asn711=
NM_001346898.2:c.2268C=	NP_001333827.1:p.Asn756=
NM_001346900.2:c.2109C=	NP_001333829.1:p.Asn703=
NM_001346941.2:c.1467C=	NP_001333870.1:p.Asn489=
NM_001346899.2:c.2133C=	NP_001333828.1:p.Asn711=