Canonical Allele Identifier: CA1708918330

Gene: EGFR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174774_55174785delinsAATTAAGAGAAG , CM000669.2:g.55174774_55174785delinsAATTAAGAGAAG	GRCh38
NC_000007.13:g.55242467_55242478delinsAATTAAGAGAAG , CM000669.1:g.55242467_55242478delinsAATTAAGAGAAG	GRCh37
NC_000007.12:g.55209961_55209972delinsAATTAAGAGAAG	NCBI36
NG_007726.3:g.160743_160754delinsAATTAAGAGAAG , LRG_304:g.160743_160754delinsAATTAAGAGAAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2078_2089delinsAATTAAGAGAAG	ENSP00000413354.2:p.Glu693=
ENST00000700145.1:c.586_597delinsAATTAAGAGAAG
ENST00000275493.7:c.2237_2248delinsAATTAAGAGAAG MANE Select	ENSP00000275493.2:p.Glu746=
ENST00000275493.6:c.2237_2248delinsAATTAAGAGAAG	ENSP00000275493.2:p.Glu746=
ENST00000442591.5:c.*28+1846_*28+1857delinsAATTAAGAGAAG	ENSP00000410031.1:n.*28+1846_*28+1857deli...
ENST00000454757.6:c.2102_2113delinsAATTAAGAGAAG	ENSP00000395243.3:p.Glu701=
ENST00000455089.5:c.2102_2113delinsAATTAAGAGAAG	ENSP00000415559.1:p.Glu701=
NM_005228.3:c.2237_2248delinsAATTAAGAGAAG , LRG_304t1:c.2237_2248delinsAATTAAGAGAAG	NP_005219.2:p.Glu746=
NM_001346897.1:c.2102_2113delinsAATTAAGAGAAG	NP_001333826.1:p.Glu701=
NM_001346898.1:c.2237_2248delinsAATTAAGAGAAG	NP_001333827.1:p.Glu746=
NM_001346899.1:c.2102_2113delinsAATTAAGAGAAG	NP_001333828.1:p.Glu701=
NM_001346900.1:c.2078_2089delinsAATTAAGAGAAG	NP_001333829.1:p.Glu693=
NM_001346941.1:c.1436_1447delinsAATTAAGAGAAG	NP_001333870.1:p.Glu479=
NM_005228.4:c.2237_2248delinsAATTAAGAGAAG	NP_005219.2:p.Glu746=
NM_005228.5:c.2237_2248delinsAATTAAGAGAAG MANE Select	NP_005219.2:p.Glu746=
NM_001346897.2:c.2102_2113delinsAATTAAGAGAAG	NP_001333826.1:p.Glu701=
NM_001346898.2:c.2237_2248delinsAATTAAGAGAAG	NP_001333827.1:p.Glu746=
NM_001346900.2:c.2078_2089delinsAATTAAGAGAAG	NP_001333829.1:p.Glu693=
NM_001346941.2:c.1436_1447delinsAATTAAGAGAAG	NP_001333870.1:p.Glu479=
NM_001346899.2:c.2102_2113delinsAATTAAGAGAAG	NP_001333828.1:p.Glu701=