Canonical Allele Identifier: CA1708910221

Gene: EGFR EGFR-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55184065A= , CM000669.2:g.55184065A=	GRCh38
NC_000007.13:g.55251758A= , CM000669.1:g.55251758A=	GRCh37
NC_000007.12:g.55219252A=	NCBI36
NG_007726.3:g.170034A= , LRG_304:g.170034A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2310+2587A= (EGFR)	ENSP00000413354.2:n.2310+2587A=
ENST00000700145.1:c.818+2587A= (EGFR)
ENST00000275493.7:c.2469+2587A= (EGFR) MANE Select	ENSP00000275493.2:n.2469+2587A=
ENST00000275493.6:c.2469+2587A= (EGFR)	ENSP00000275493.2:n.2469+2587A=
ENST00000442591.5:c.*28+11137A= (EGFR)	ENSP00000410031.1:n.*28+11137A=
ENST00000454757.6:c.2334+2587A= (EGFR)	ENSP00000395243.3:n.2334+2587A=
ENST00000455089.5:c.2334+2587A= (EGFR)	ENSP00000415559.1:n.2334+2587A=
NM_005228.3:c.2469+2587A= , LRG_304t1:c.2469+2587A= (EGFR)	NP_005219.2:n.2469+2587A=
NR_047551.1:n.94-1588T= (EGFR-AS1)
NM_001346897.1:c.2334+2587A= (EGFR)	NP_001333826.1:n.2334+2587A=
NM_001346898.1:c.2469+2587A= (EGFR)	NP_001333827.1:n.2469+2587A=
NM_001346899.1:c.2334+2587A= (EGFR)	NP_001333828.1:n.2334+2587A=
NM_001346900.1:c.2310+2587A= (EGFR)	NP_001333829.1:n.2310+2587A=
NM_001346941.1:c.1668+2587A= (EGFR)	NP_001333870.1:n.1668+2587A=
NM_005228.4:c.2469+2587A= (EGFR)	NP_005219.2:n.2469+2587A=
NM_005228.5:c.2469+2587A= (EGFR) MANE Select	NP_005219.2:n.2469+2587A=
NM_001346897.2:c.2334+2587A= (EGFR)	NP_001333826.1:n.2334+2587A=
NM_001346898.2:c.2469+2587A= (EGFR)	NP_001333827.1:n.2469+2587A=
NM_001346900.2:c.2310+2587A= (EGFR)	NP_001333829.1:n.2310+2587A=
NM_001346941.2:c.1668+2587A= (EGFR)	NP_001333870.1:n.1668+2587A=
NM_001346899.2:c.2334+2587A= (EGFR)	NP_001333828.1:n.2334+2587A=