Canonical Allele Identifier: CA1708918347

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174782G= , CM000669.2:g.55174782G=	GRCh38
NC_000007.13:g.55242475G= , CM000669.1:g.55242475G=	GRCh37
NC_000007.12:g.55209969G=	NCBI36
NG_007726.3:g.160751G= , LRG_304:g.160751G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2086G=	ENSP00000413354.2:p.Glu696=
ENST00000700145.1:c.594G=
ENST00000275493.7:c.2245G= MANE Select	ENSP00000275493.2:p.Glu749=
ENST00000275493.6:c.2245G=	ENSP00000275493.2:p.Glu749=
ENST00000442591.5:c.*28+1854G=	ENSP00000410031.1:n.*28+1854G=
ENST00000454757.6:c.2110G=	ENSP00000395243.3:p.Glu704=
ENST00000455089.5:c.2110G=	ENSP00000415559.1:p.Glu704=
NM_005228.3:c.2245G= , LRG_304t1:c.2245G=	NP_005219.2:p.Glu749=
NM_001346897.1:c.2110G=	NP_001333826.1:p.Glu704=
NM_001346898.1:c.2245G=	NP_001333827.1:p.Glu749=
NM_001346899.1:c.2110G=	NP_001333828.1:p.Glu704=
NM_001346900.1:c.2086G=	NP_001333829.1:p.Glu696=
NM_001346941.1:c.1444G=	NP_001333870.1:p.Glu482=
NM_005228.4:c.2245G=	NP_005219.2:p.Glu749=
NM_005228.5:c.2245G= MANE Select	NP_005219.2:p.Glu749=
NM_001346897.2:c.2110G=	NP_001333826.1:p.Glu704=
NM_001346898.2:c.2245G=	NP_001333827.1:p.Glu749=
NM_001346900.2:c.2086G=	NP_001333829.1:p.Glu696=
NM_001346941.2:c.1444G=	NP_001333870.1:p.Glu482=
NM_001346899.2:c.2110G=	NP_001333828.1:p.Glu704=