Canonical Allele Identifier: CA1708922214

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55191566C= , CM000669.2:g.55191566C=	GRCh38
NC_000007.13:g.55259259C= , CM000669.1:g.55259259C=	GRCh37
NC_000007.12:g.55226753C=	NCBI36
NG_007726.3:g.177535C= , LRG_304:g.177535C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2311-153C=	ENSP00000413354.2:n.2311-153C=
ENST00000700145.1:c.819-153C=
ENST00000275493.7:c.2470-153C= MANE Select	ENSP00000275493.2:n.2470-153C=
ENST00000275493.6:c.2470-153C=	ENSP00000275493.2:n.2470-153C=
ENST00000442591.5:c.*28+18638C=	ENSP00000410031.1:n.*28+18638C=
ENST00000454757.6:c.2335-153C=	ENSP00000395243.3:n.2335-153C=
ENST00000455089.5:c.2335-153C=	ENSP00000415559.1:n.2335-153C=
NM_005228.3:c.2470-153C= , LRG_304t1:c.2470-153C=	NP_005219.2:n.2470-153C=
NM_001346897.1:c.2335-153C=	NP_001333826.1:n.2335-153C=
NM_001346898.1:c.2470-153C=	NP_001333827.1:n.2470-153C=
NM_001346899.1:c.2335-153C=	NP_001333828.1:n.2335-153C=
NM_001346900.1:c.2311-153C=	NP_001333829.1:n.2311-153C=
NM_001346941.1:c.1669-153C=	NP_001333870.1:n.1669-153C=
NM_005228.4:c.2470-153C=	NP_005219.2:n.2470-153C=
NM_005228.5:c.2470-153C= MANE Select	NP_005219.2:n.2470-153C=
NM_001346897.2:c.2335-153C=	NP_001333826.1:n.2335-153C=
NM_001346898.2:c.2470-153C=	NP_001333827.1:n.2470-153C=
NM_001346900.2:c.2311-153C=	NP_001333829.1:n.2311-153C=
NM_001346941.2:c.1669-153C=	NP_001333870.1:n.1669-153C=
NM_001346899.2:c.2335-153C=	NP_001333828.1:n.2335-153C=