Canonical Allele Identifier: CA1708922865

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55192030A= , CM000669.2:g.55192030A=	GRCh38
NC_000007.13:g.55259723A= , CM000669.1:g.55259723A=	GRCh37
NC_000007.12:g.55227217A=	NCBI36
NG_007726.3:g.177999A= , LRG_304:g.177999A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2466+156A=	ENSP00000413354.2:n.2466+156A=
ENST00000700145.1:c.899+231A=
ENST00000275493.7:c.2625+156A= MANE Select	ENSP00000275493.2:n.2625+156A=
ENST00000275493.6:c.2625+156A=	ENSP00000275493.2:n.2625+156A=
ENST00000442591.5:c.*28+19102A=	ENSP00000410031.1:n.*28+19102A=
ENST00000454757.6:c.2490+156A=	ENSP00000395243.3:n.2490+156A=
ENST00000455089.5:c.2490+156A=	ENSP00000415559.1:n.2490+156A=
NM_005228.3:c.2625+156A= , LRG_304t1:c.2625+156A=	NP_005219.2:n.2625+156A=
NM_001346897.1:c.2490+156A=	NP_001333826.1:n.2490+156A=
NM_001346898.1:c.2625+156A=	NP_001333827.1:n.2625+156A=
NM_001346899.1:c.2490+156A=	NP_001333828.1:n.2490+156A=
NM_001346900.1:c.2466+156A=	NP_001333829.1:n.2466+156A=
NM_001346941.1:c.1824+156A=	NP_001333870.1:n.1824+156A=
NM_005228.4:c.2625+156A=	NP_005219.2:n.2625+156A=
NM_005228.5:c.2625+156A= MANE Select	NP_005219.2:n.2625+156A=
NM_001346897.2:c.2490+156A=	NP_001333826.1:n.2490+156A=
NM_001346898.2:c.2625+156A=	NP_001333827.1:n.2625+156A=
NM_001346900.2:c.2466+156A=	NP_001333829.1:n.2466+156A=
NM_001346941.2:c.1824+156A=	NP_001333870.1:n.1824+156A=
NM_001346899.2:c.2490+156A=	NP_001333828.1:n.2490+156A=