Canonical Allele Identifier: CA1708918296

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174757T= , CM000669.2:g.55174757T=	GRCh38
NC_000007.13:g.55242450T= , CM000669.1:g.55242450T=	GRCh37
NC_000007.12:g.55209944T=	NCBI36
NG_007726.3:g.160726T= , LRG_304:g.160726T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2061T=	ENSP00000413354.2:p.Ile687=
ENST00000700145.1:c.569T=
ENST00000275493.7:c.2220T= MANE Select	ENSP00000275493.2:p.Ile740=
ENST00000275493.6:c.2220T=	ENSP00000275493.2:p.Ile740=
ENST00000442591.5:c.*28+1829T=	ENSP00000410031.1:n.*28+1829T=
ENST00000454757.6:c.2085T=	ENSP00000395243.3:p.Ile695=
ENST00000455089.5:c.2085T=	ENSP00000415559.1:p.Ile695=
NM_005228.3:c.2220T= , LRG_304t1:c.2220T=	NP_005219.2:p.Ile740=
NM_001346897.1:c.2085T=	NP_001333826.1:p.Ile695=
NM_001346898.1:c.2220T=	NP_001333827.1:p.Ile740=
NM_001346899.1:c.2085T=	NP_001333828.1:p.Ile695=
NM_001346900.1:c.2061T=	NP_001333829.1:p.Ile687=
NM_001346941.1:c.1419T=	NP_001333870.1:p.Ile473=
NM_005228.4:c.2220T=	NP_005219.2:p.Ile740=
NM_005228.5:c.2220T= MANE Select	NP_005219.2:p.Ile740=
NM_001346897.2:c.2085T=	NP_001333826.1:p.Ile695=
NM_001346898.2:c.2220T=	NP_001333827.1:p.Ile740=
NM_001346900.2:c.2061T=	NP_001333829.1:p.Ile687=
NM_001346941.2:c.1419T=	NP_001333870.1:p.Ile473=
NM_001346899.2:c.2085T=	NP_001333828.1:p.Ile695=