Canonical Allele Identifier: CA182031

Gene: EGFR

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174774_55174783delinsC , CM000669.2:g.55174774_55174783delinsC	GRCh38
NC_000007.13:g.55242467_55242476delinsC , CM000669.1:g.55242467_55242476delinsC	GRCh37
NC_000007.12:g.55209961_55209970delinsC	NCBI36
NG_007726.3:g.160743_160752delinsC , LRG_304:g.160743_160752delinsC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2078_2087delinsC	ENSP00000413354.2:p.Glu693_Glu696delinsAla
ENST00000700145.1:c.586_595delinsC
ENST00000275493.7:c.2237_2246delinsC MANE Select	ENSP00000275493.2:p.Glu746_Glu749delinsAla
ENST00000275493.6:c.2237_2246delinsC	ENSP00000275493.2:p.Glu746_Glu749delinsAla
ENST00000442591.5:c.*28+1846_*28+1855delinsC	ENSP00000410031.1:n.*28+1846_*28+1855delinsC
ENST00000454757.6:c.2102_2111delinsC	ENSP00000395243.3:p.Glu701_Glu704delinsAla
ENST00000455089.5:c.2102_2111delinsC	ENSP00000415559.1:p.Glu701_Glu704delinsAla
NM_005228.3:c.2237_2246delinsC , LRG_304t1:c.2237_2246delinsC	NP_005219.2:p.Glu746_Glu749delinsAla
NM_001346897.1:c.2102_2111delinsC	NP_001333826.1:p.Glu701_Glu704delinsAla
NM_001346898.1:c.2237_2246delinsC	NP_001333827.1:p.Glu746_Glu749delinsAla
NM_001346899.1:c.2102_2111delinsC	NP_001333828.1:p.Glu701_Glu704delinsAla
NM_001346900.1:c.2078_2087delinsC	NP_001333829.1:p.Glu693_Glu696delinsAla
NM_001346941.1:c.1436_1445delinsC	NP_001333870.1:p.Glu479_Glu482delinsAla
NM_005228.4:c.2237_2246delinsC	NP_005219.2:p.Glu746_Glu749delinsAla
NM_005228.5:c.2237_2246delinsC MANE Select	NP_005219.2:p.Glu746_Glu749delinsAla
NM_001346897.2:c.2102_2111delinsC	NP_001333826.1:p.Glu701_Glu704delinsAla
NM_001346898.2:c.2237_2246delinsC	NP_001333827.1:p.Glu746_Glu749delinsAla
NM_001346900.2:c.2078_2087delinsC	NP_001333829.1:p.Glu693_Glu696delinsAla
NM_001346941.2:c.1436_1445delinsC	NP_001333870.1:p.Glu479_Glu482delinsAla
NM_001346899.2:c.2102_2111delinsC	NP_001333828.1:p.Glu701_Glu704delinsAla