Canonical Allele Identifier: CA1708928326

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55201039C= , CM000669.2:g.55201039C=	GRCh38
NC_000007.13:g.55268732C= , CM000669.1:g.55268732C=	GRCh37
NC_000007.12:g.55236226C=	NCBI36
NG_007726.3:g.187008C= , LRG_304:g.187008C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2788-149C=	ENSP00000413354.2:n.2788-149C=
ENST00000700145.1:c.900-4308C=
ENST00000700146.1:n.691-149C=
ENST00000700147.1:n.467C=
ENST00000275493.7:c.2947-149C= MANE Select	ENSP00000275493.2:n.2947-149C=
ENST00000275493.6:c.2947-149C=	ENSP00000275493.2:n.2947-149C=
ENST00000442591.5:c.*28+28111C=	ENSP00000410031.1:n.*28+28111C=
ENST00000454757.6:c.2812-149C=	ENSP00000395243.3:n.2812-149C=
ENST00000455089.5:c.2812-149C=	ENSP00000415559.1:n.2812-149C=
NM_005228.3:c.2947-149C= , LRG_304t1:c.2947-149C=	NP_005219.2:n.2947-149C=
NM_001346897.1:c.2812-149C=	NP_001333826.1:n.2812-149C=
NM_001346898.1:c.2947-149C=	NP_001333827.1:n.2947-149C=
NM_001346899.1:c.2812-149C=	NP_001333828.1:n.2812-149C=
NM_001346900.1:c.2788-149C=	NP_001333829.1:n.2788-149C=
NM_001346941.1:c.2146-149C=	NP_001333870.1:n.2146-149C=
NM_005228.4:c.2947-149C=	NP_005219.2:n.2947-149C=
NM_005228.5:c.2947-149C= MANE Select	NP_005219.2:n.2947-149C=
NM_001346897.2:c.2812-149C=	NP_001333826.1:n.2812-149C=
NM_001346898.2:c.2947-149C=	NP_001333827.1:n.2947-149C=
NM_001346900.2:c.2788-149C=	NP_001333829.1:n.2788-149C=
NM_001346941.2:c.2146-149C=	NP_001333870.1:n.2146-149C=
NM_001346899.2:c.2812-149C=	NP_001333828.1:n.2812-149C=