Canonical Allele Identifier: CA1708922557

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55191786A= , CM000669.2:g.55191786A=	GRCh38
NC_000007.13:g.55259479A= , CM000669.1:g.55259479A=	GRCh37
NC_000007.12:g.55226973A=	NCBI36
NG_007726.3:g.177755A= , LRG_304:g.177755A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2378A=	ENSP00000413354.2:p.Lys793=
ENST00000700145.1:c.886A=
ENST00000275493.7:c.2537A= MANE Select	ENSP00000275493.2:p.Lys846=
ENST00000275493.6:c.2537A=	ENSP00000275493.2:p.Lys846=
ENST00000442591.5:c.*28+18858A=	ENSP00000410031.1:n.*28+18858A=
ENST00000454757.6:c.2402A=	ENSP00000395243.3:p.Lys801=
ENST00000455089.5:c.2402A=	ENSP00000415559.1:p.Lys801=
NM_005228.3:c.2537A= , LRG_304t1:c.2537A=	NP_005219.2:p.Lys846=
NM_001346897.1:c.2402A=	NP_001333826.1:p.Lys801=
NM_001346898.1:c.2537A=	NP_001333827.1:p.Lys846=
NM_001346899.1:c.2402A=	NP_001333828.1:p.Lys801=
NM_001346900.1:c.2378A=	NP_001333829.1:p.Lys793=
NM_001346941.1:c.1736A=	NP_001333870.1:p.Lys579=
NM_005228.4:c.2537A=	NP_005219.2:p.Lys846=
NM_005228.5:c.2537A= MANE Select	NP_005219.2:p.Lys846=
NM_001346897.2:c.2402A=	NP_001333826.1:p.Lys801=
NM_001346898.2:c.2537A=	NP_001333827.1:p.Lys846=
NM_001346900.2:c.2378A=	NP_001333829.1:p.Lys793=
NM_001346941.2:c.1736A=	NP_001333870.1:p.Lys579=
NM_001346899.2:c.2402A=	NP_001333828.1:p.Lys801=