Canonical Allele Identifier: CA1708928449

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55201274G= , CM000669.2:g.55201274G=	GRCh38
NC_000007.13:g.55268967G= , CM000669.1:g.55268967G=	GRCh37
NC_000007.12:g.55236461G=	NCBI36
NG_007726.3:g.187243G= , LRG_304:g.187243G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2874G=	ENSP00000413354.2:p.Val958=
ENST00000700145.1:c.900-4073G=
ENST00000700146.1:n.777G=
ENST00000700147.1:n.702G=
ENST00000275493.7:c.3033G= MANE Select	ENSP00000275493.2:p.Val1011=
ENST00000275493.6:c.3033G=	ENSP00000275493.2:p.Val1011=
ENST00000442591.5:c.*28+28346G=	ENSP00000410031.1:n.*28+28346G=
ENST00000454757.6:c.2898G=	ENSP00000395243.3:p.Val966=
ENST00000455089.5:c.2898G=	ENSP00000415559.1:p.Val966=
NM_005228.3:c.3033G= , LRG_304t1:c.3033G=	NP_005219.2:p.Val1011=
NM_001346897.1:c.2898G=	NP_001333826.1:p.Val966=
NM_001346898.1:c.3033G=	NP_001333827.1:p.Val1011=
NM_001346899.1:c.2898G=	NP_001333828.1:p.Val966=
NM_001346900.1:c.2874G=	NP_001333829.1:p.Val958=
NM_001346941.1:c.2232G=	NP_001333870.1:p.Val744=
NM_005228.4:c.3033G=	NP_005219.2:p.Val1011=
NM_005228.5:c.3033G= MANE Select	NP_005219.2:p.Val1011=
NM_001346897.2:c.2898G=	NP_001333826.1:p.Val966=
NM_001346898.2:c.3033G=	NP_001333827.1:p.Val1011=
NM_001346900.2:c.2874G=	NP_001333829.1:p.Val958=
NM_001346941.2:c.2232G=	NP_001333870.1:p.Val744=
NM_001346899.2:c.2898G=	NP_001333828.1:p.Val966=