Canonical Allele Identifier: CA1708928008

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55200396C= , CM000669.2:g.55200396C=	GRCh38
NC_000007.13:g.55268089C= , CM000669.1:g.55268089C=	GRCh37
NC_000007.12:g.55235583C=	NCBI36
NG_007726.3:g.186365C= , LRG_304:g.186365C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2770C=	ENSP00000413354.2:p.Arg924=
ENST00000700145.1:c.900-4951C=
ENST00000700146.1:n.673C=
ENST00000275493.7:c.2929C= MANE Select	ENSP00000275493.2:p.Arg977=
ENST00000275493.6:c.2929C=	ENSP00000275493.2:p.Arg977=
ENST00000442591.5:c.*28+27468C=	ENSP00000410031.1:n.*28+27468C=
ENST00000454757.6:c.2794C=	ENSP00000395243.3:p.Arg932=
ENST00000455089.5:c.2794C=	ENSP00000415559.1:p.Arg932=
ENST00000485503.1:n.259C=
NM_005228.3:c.2929C= , LRG_304t1:c.2929C=	NP_005219.2:p.Arg977=
NM_001346897.1:c.2794C=	NP_001333826.1:p.Arg932=
NM_001346898.1:c.2929C=	NP_001333827.1:p.Arg977=
NM_001346899.1:c.2794C=	NP_001333828.1:p.Arg932=
NM_001346900.1:c.2770C=	NP_001333829.1:p.Arg924=
NM_001346941.1:c.2128C=	NP_001333870.1:p.Arg710=
NM_005228.4:c.2929C=	NP_005219.2:p.Arg977=
NM_005228.5:c.2929C= MANE Select	NP_005219.2:p.Arg977=
NM_001346897.2:c.2794C=	NP_001333826.1:p.Arg932=
NM_001346898.2:c.2929C=	NP_001333827.1:p.Arg977=
NM_001346900.2:c.2770C=	NP_001333829.1:p.Arg924=
NM_001346941.2:c.2128C=	NP_001333870.1:p.Arg710=
NM_001346899.2:c.2794C=	NP_001333828.1:p.Arg932=