Canonical Allele Identifier: CA1708918359

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174791T= , CM000669.2:g.55174791T=	GRCh38
NC_000007.13:g.55242484T= , CM000669.1:g.55242484T=	GRCh37
NC_000007.12:g.55209978T=	NCBI36
NG_007726.3:g.160760T= , LRG_304:g.160760T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2095T=	ENSP00000413354.2:p.Ser699=
ENST00000700145.1:c.603T=
ENST00000275493.7:c.2254T= MANE Select	ENSP00000275493.2:p.Ser752=
ENST00000275493.6:c.2254T=	ENSP00000275493.2:p.Ser752=
ENST00000442591.5:c.*28+1863T=	ENSP00000410031.1:n.*28+1863T=
ENST00000454757.6:c.2119T=	ENSP00000395243.3:p.Ser707=
ENST00000455089.5:c.2119T=	ENSP00000415559.1:p.Ser707=
NM_005228.3:c.2254T= , LRG_304t1:c.2254T=	NP_005219.2:p.Ser752=
NM_001346897.1:c.2119T=	NP_001333826.1:p.Ser707=
NM_001346898.1:c.2254T=	NP_001333827.1:p.Ser752=
NM_001346899.1:c.2119T=	NP_001333828.1:p.Ser707=
NM_001346900.1:c.2095T=	NP_001333829.1:p.Ser699=
NM_001346941.1:c.1453T=	NP_001333870.1:p.Ser485=
NM_005228.4:c.2254T=	NP_005219.2:p.Ser752=
NM_005228.5:c.2254T= MANE Select	NP_005219.2:p.Ser752=
NM_001346897.2:c.2119T=	NP_001333826.1:p.Ser707=
NM_001346898.2:c.2254T=	NP_001333827.1:p.Ser752=
NM_001346900.2:c.2095T=	NP_001333829.1:p.Ser699=
NM_001346941.2:c.1453T=	NP_001333870.1:p.Ser485=
NM_001346899.2:c.2119T=	NP_001333828.1:p.Ser707=