Canonical Allele Identifier: CA1708918297

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174760C= , CM000669.2:g.55174760C=	GRCh38
NC_000007.13:g.55242453C= , CM000669.1:g.55242453C=	GRCh37
NC_000007.12:g.55209947C=	NCBI36
NG_007726.3:g.160729C= , LRG_304:g.160729C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2064C=	ENSP00000413354.2:p.Pro688=
ENST00000700145.1:c.572C=
ENST00000275493.7:c.2223C= MANE Select	ENSP00000275493.2:p.Pro741=
ENST00000275493.6:c.2223C=	ENSP00000275493.2:p.Pro741=
ENST00000442591.5:c.*28+1832C=	ENSP00000410031.1:n.*28+1832C=
ENST00000454757.6:c.2088C=	ENSP00000395243.3:p.Pro696=
ENST00000455089.5:c.2088C=	ENSP00000415559.1:p.Pro696=
NM_005228.3:c.2223C= , LRG_304t1:c.2223C=	NP_005219.2:p.Pro741=
NM_001346897.1:c.2088C=	NP_001333826.1:p.Pro696=
NM_001346898.1:c.2223C=	NP_001333827.1:p.Pro741=
NM_001346899.1:c.2088C=	NP_001333828.1:p.Pro696=
NM_001346900.1:c.2064C=	NP_001333829.1:p.Pro688=
NM_001346941.1:c.1422C=	NP_001333870.1:p.Pro474=
NM_005228.4:c.2223C=	NP_005219.2:p.Pro741=
NM_005228.5:c.2223C= MANE Select	NP_005219.2:p.Pro741=
NM_001346897.2:c.2088C=	NP_001333826.1:p.Pro696=
NM_001346898.2:c.2223C=	NP_001333827.1:p.Pro741=
NM_001346900.2:c.2064C=	NP_001333829.1:p.Pro688=
NM_001346941.2:c.1422C=	NP_001333870.1:p.Pro474=
NM_001346899.2:c.2088C=	NP_001333828.1:p.Pro696=