Canonical Allele Identifier: CA1708931606

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55206391T= , CM000669.2:g.55206391T=	GRCh38
NC_000007.13:g.55274084T= , CM000669.1:g.55274084T=	GRCh37
NC_000007.12:g.55241578T=	NCBI36
NG_007726.3:g.192360T= , LRG_304:g.192360T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.*774T=	ENSP00000413354.2:n.*774T=
ENST00000700146.1:n.2151T=
ENST00000275493.7:c.*774T= MANE Select	ENSP00000275493.2:n.*774T=
ENST00000275493.6:c.*774T=	ENSP00000275493.2:n.*774T=
ENST00000442591.5:c.*28+33463T=	ENSP00000410031.1:n.*28+33463T=
ENST00000454757.6:c.*774T=	ENSP00000395243.3:n.*774T=
NM_005228.3:c.*774T= , LRG_304t1:c.*774T=	NP_005219.2:n.*774T=
NM_001346899.1:c.*774T=	NP_001333828.1:n.*774T=
NM_001346900.1:c.*774T=	NP_001333829.1:n.*774T=
NM_001346941.1:c.*774T=	NP_001333870.1:n.*774T=
NM_005228.4:c.*774T=	NP_005219.2:n.*774T=
NM_005228.5:c.*774T= MANE Select	NP_005219.2:n.*774T=
NM_001346900.2:c.*774T=	NP_001333829.1:n.*774T=
NM_001346941.2:c.*774T=	NP_001333870.1:n.*774T=
NM_001346899.2:c.*774T=	NP_001333828.1:n.*774T=