Canonical Allele Identifier: CA1708905707

Gene: EGFR EGFR-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55181444A= , CM000669.2:g.55181444A=	GRCh38
NC_000007.13:g.55249137A= , CM000669.1:g.55249137A=	GRCh37
NC_000007.12:g.55216631A=	NCBI36
NG_007726.3:g.167413A= , LRG_304:g.167413A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2276A= (EGFR)	ENSP00000413354.2:p.Gln759=
ENST00000700145.1:c.784A= (EGFR)
ENST00000275493.7:c.2435A= (EGFR) MANE Select	ENSP00000275493.2:p.Gln812=
ENST00000275493.6:c.2435A= (EGFR)	ENSP00000275493.2:p.Gln812=
ENST00000442591.5:c.*28+8516A= (EGFR)	ENSP00000410031.1:n.*28+8516A=
ENST00000454757.6:c.2300A= (EGFR)	ENSP00000395243.3:p.Gln767=
ENST00000455089.5:c.2300A= (EGFR)	ENSP00000415559.1:p.Gln767=
NM_005228.3:c.2435A= , LRG_304t1:c.2435A= (EGFR)	NP_005219.2:p.Gln812=
NR_047551.1:n.1127T= (EGFR-AS1)
NM_001346897.1:c.2300A= (EGFR)	NP_001333826.1:p.Gln767=
NM_001346898.1:c.2435A= (EGFR)	NP_001333827.1:p.Gln812=
NM_001346899.1:c.2300A= (EGFR)	NP_001333828.1:p.Gln767=
NM_001346900.1:c.2276A= (EGFR)	NP_001333829.1:p.Gln759=
NM_001346941.1:c.1634A= (EGFR)	NP_001333870.1:p.Gln545=
NM_005228.4:c.2435A= (EGFR)	NP_005219.2:p.Gln812=
NM_005228.5:c.2435A= (EGFR) MANE Select	NP_005219.2:p.Gln812=
NM_001346897.2:c.2300A= (EGFR)	NP_001333826.1:p.Gln767=
NM_001346898.2:c.2435A= (EGFR)	NP_001333827.1:p.Gln812=
NM_001346900.2:c.2276A= (EGFR)	NP_001333829.1:p.Gln759=
NM_001346941.2:c.1634A= (EGFR)	NP_001333870.1:p.Gln545=
NM_001346899.2:c.2300A= (EGFR)	NP_001333828.1:p.Gln767=