Canonical Allele Identifier: CA181002
Gene: EGFR HGNC NCBI

Linked Data

ClinVar Variation Id: 177920
ClinVar RCV Id: RCV000154579
dbSNP Id: rs727504402
COSMIC: COSM26680

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174773_55174789delinsAT , CM000669.2:g.55174773_55174789delinsAT GRCh38
NC_000007.13:g.55242466_55242482delinsAT , CM000669.1:g.55242466_55242482delinsAT GRCh37
NC_000007.12:g.55209960_55209976delinsAT NCBI36
NG_007726.3:g.160742_160758delinsAT , LRG_304:g.160742_160758delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2077_2093delinsAT ENSP00000413354.2:p.Glu693_Thr698delinsIl...
ENST00000700145.1:c.585_601delinsAT
ENST00000275493.7:c.2236_2252delinsAT MANE Select ENSP00000275493.2:p.Glu746_Thr751delinsIl...
ENST00000275493.6:c.2236_2252delinsAT ENSP00000275493.2:p.Glu746_Thr751delinsIl...
ENST00000442591.5:c.*28+1845_*28+1861delinsAT ENSP00000410031.1:n.*28+1845_*28+1861deli...
ENST00000454757.6:c.2101_2117delinsAT ENSP00000395243.3:p.Glu701_Thr706delinsIl...
ENST00000455089.5:c.2101_2117delinsAT ENSP00000415559.1:p.Glu701_Thr706delinsIl...
NM_005228.3:c.2236_2252delinsAT , LRG_304t1:c.2236_2252delinsAT NP_005219.2:p.Glu746_Thr751delinsIle
NM_001346897.1:c.2101_2117delinsAT NP_001333826.1:p.Glu701_Thr706delinsIle
NM_001346898.1:c.2236_2252delinsAT NP_001333827.1:p.Glu746_Thr751delinsIle
NM_001346899.1:c.2101_2117delinsAT NP_001333828.1:p.Glu701_Thr706delinsIle
NM_001346900.1:c.2077_2093delinsAT NP_001333829.1:p.Glu693_Thr698delinsIle
NM_001346941.1:c.1435_1451delinsAT NP_001333870.1:p.Glu479_Thr484delinsIle
NM_005228.4:c.2236_2252delinsAT NP_005219.2:p.Glu746_Thr751delinsIle
NM_005228.5:c.2236_2252delinsAT MANE Select NP_005219.2:p.Glu746_Thr751delinsIle
NM_001346897.2:c.2101_2117delinsAT NP_001333826.1:p.Glu701_Thr706delinsIle
NM_001346898.2:c.2236_2252delinsAT NP_001333827.1:p.Glu746_Thr751delinsIle
NM_001346900.2:c.2077_2093delinsAT NP_001333829.1:p.Glu693_Thr698delinsIle
NM_001346941.2:c.1435_1451delinsAT NP_001333870.1:p.Glu479_Thr484delinsIle
NM_001346899.2:c.2101_2117delinsAT NP_001333828.1:p.Glu701_Thr706delinsIle