Canonical Allele Identifier: CA645561522
Gene: EGFR HGNC NCBI

Linked Data

dbSNP Id: rs121913435
COSMIC: COSM18428

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174775_55174785delinsTC , CM000669.2:g.55174775_55174785delinsTC GRCh38
NC_000007.13:g.55242468_55242478delinsTC , CM000669.1:g.55242468_55242478delinsTC GRCh37
NC_000007.12:g.55209962_55209972delinsTC NCBI36
NG_007726.3:g.160744_160754delinsTC , LRG_304:g.160744_160754delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2079_2089delinsTC ENSP00000413354.2:p.Glu693_Ala697delinsAs...
ENST00000700145.1:c.587_597delinsTC
ENST00000275493.7:c.2238_2248delinsTC MANE Select ENSP00000275493.2:p.Glu746_Ala750delinsAs...
ENST00000275493.6:c.2238_2248delinsTC ENSP00000275493.2:p.Glu746_Ala750delinsAs...
ENST00000442591.5:c.*28+1847_*28+1857delinsTC ENSP00000410031.1:n.*28+1847_*28+1857deli...
ENST00000454757.6:c.2103_2113delinsTC ENSP00000395243.3:p.Glu701_Ala705delinsAs...
ENST00000455089.5:c.2103_2113delinsTC ENSP00000415559.1:p.Glu701_Ala705delinsAs...
NM_005228.3:c.2238_2248delinsTC , LRG_304t1:c.2238_2248delinsTC NP_005219.2:p.Glu746_Ala750delinsAspPro
NM_001346897.1:c.2103_2113delinsTC NP_001333826.1:p.Glu701_Ala705delinsAspPr...
NM_001346898.1:c.2238_2248delinsTC NP_001333827.1:p.Glu746_Ala750delinsAspPr...
NM_001346899.1:c.2103_2113delinsTC NP_001333828.1:p.Glu701_Ala705delinsAspPr...
NM_001346900.1:c.2079_2089delinsTC NP_001333829.1:p.Glu693_Ala697delinsAspPr...
NM_001346941.1:c.1437_1447delinsTC NP_001333870.1:p.Glu479_Ala483delinsAspPr...
NM_005228.4:c.2238_2248delinsTC NP_005219.2:p.Glu746_Ala750delinsAspPro
NM_005228.5:c.2238_2248delinsTC MANE Select NP_005219.2:p.Glu746_Ala750delinsAspPro
NM_001346897.2:c.2103_2113delinsTC NP_001333826.1:p.Glu701_Ala705delinsAspPr...
NM_001346898.2:c.2238_2248delinsTC NP_001333827.1:p.Glu746_Ala750delinsAspPr...
NM_001346900.2:c.2079_2089delinsTC NP_001333829.1:p.Glu693_Ala697delinsAspPr...
NM_001346941.2:c.1437_1447delinsTC NP_001333870.1:p.Glu479_Ala483delinsAspPr...
NM_001346899.2:c.2103_2113delinsTC NP_001333828.1:p.Glu701_Ala705delinsAspPr...