Canonical Allele Identifier: CA1708928465

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55201306G= , CM000669.2:g.55201306G=	GRCh38
NC_000007.13:g.55268999G= , CM000669.1:g.55268999G=	GRCh37
NC_000007.12:g.55236493G=	NCBI36
NG_007726.3:g.187275G= , LRG_304:g.187275G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2906G=	ENSP00000413354.2:p.Gly969=
ENST00000700145.1:c.900-4041G=
ENST00000700146.1:n.809G=
ENST00000700147.1:n.734G=
ENST00000275493.7:c.3065G= MANE Select	ENSP00000275493.2:p.Gly1022=
ENST00000275493.6:c.3065G=	ENSP00000275493.2:p.Gly1022=
ENST00000442591.5:c.*28+28378G=	ENSP00000410031.1:n.*28+28378G=
ENST00000454757.6:c.2930G=	ENSP00000395243.3:p.Gly977=
ENST00000455089.5:c.2930G=	ENSP00000415559.1:p.Gly977=
NM_005228.3:c.3065G= , LRG_304t1:c.3065G=	NP_005219.2:p.Gly1022=
NM_001346897.1:c.2930G=	NP_001333826.1:p.Gly977=
NM_001346898.1:c.3065G=	NP_001333827.1:p.Gly1022=
NM_001346899.1:c.2930G=	NP_001333828.1:p.Gly977=
NM_001346900.1:c.2906G=	NP_001333829.1:p.Gly969=
NM_001346941.1:c.2264G=	NP_001333870.1:p.Gly755=
NM_005228.4:c.3065G=	NP_005219.2:p.Gly1022=
NM_005228.5:c.3065G= MANE Select	NP_005219.2:p.Gly1022=
NM_001346897.2:c.2930G=	NP_001333826.1:p.Gly977=
NM_001346898.2:c.3065G=	NP_001333827.1:p.Gly1022=
NM_001346900.2:c.2906G=	NP_001333829.1:p.Gly969=
NM_001346941.2:c.2264G=	NP_001333870.1:p.Gly755=
NM_001346899.2:c.2930G=	NP_001333828.1:p.Gly977=