Canonical Allele Identifier: CA1708928440

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55201260A= , CM000669.2:g.55201260A=	GRCh38
NC_000007.13:g.55268953A= , CM000669.1:g.55268953A=	GRCh37
NC_000007.12:g.55236447A=	NCBI36
NG_007726.3:g.187229A= , LRG_304:g.187229A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2860A=	ENSP00000413354.2:p.Met954=
ENST00000700145.1:c.900-4087A=
ENST00000700146.1:n.763A=
ENST00000700147.1:n.688A=
ENST00000275493.7:c.3019A= MANE Select	ENSP00000275493.2:p.Met1007=
ENST00000275493.6:c.3019A=	ENSP00000275493.2:p.Met1007=
ENST00000442591.5:c.*28+28332A=	ENSP00000410031.1:n.*28+28332A=
ENST00000454757.6:c.2884A=	ENSP00000395243.3:p.Met962=
ENST00000455089.5:c.2884A=	ENSP00000415559.1:p.Met962=
NM_005228.3:c.3019A= , LRG_304t1:c.3019A=	NP_005219.2:p.Met1007=
NM_001346897.1:c.2884A=	NP_001333826.1:p.Met962=
NM_001346898.1:c.3019A=	NP_001333827.1:p.Met1007=
NM_001346899.1:c.2884A=	NP_001333828.1:p.Met962=
NM_001346900.1:c.2860A=	NP_001333829.1:p.Met954=
NM_001346941.1:c.2218A=	NP_001333870.1:p.Met740=
NM_005228.4:c.3019A=	NP_005219.2:p.Met1007=
NM_005228.5:c.3019A= MANE Select	NP_005219.2:p.Met1007=
NM_001346897.2:c.2884A=	NP_001333826.1:p.Met962=
NM_001346898.2:c.3019A=	NP_001333827.1:p.Met1007=
NM_001346900.2:c.2860A=	NP_001333829.1:p.Met954=
NM_001346941.2:c.2218A=	NP_001333870.1:p.Met740=
NM_001346899.2:c.2884A=	NP_001333828.1:p.Met962=