Canonical Allele Identifier: CA645561512
Gene: EGFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174774_55174789delinsT , CM000669.2:g.55174774_55174789delinsT GRCh38
NC_000007.13:g.55242467_55242482delinsT , CM000669.1:g.55242467_55242482delinsT GRCh37
NC_000007.12:g.55209961_55209976delinsT NCBI36
NG_007726.3:g.160743_160758delinsT , LRG_304:g.160743_160758delinsT

Transcript Alleles

HGVS Amino-acid Change
ENST00000450046.2:c.2078_2093delinsT ENSP00000413354.2:p.Glu693_Thr698delinsVal
ENST00000700145.1:c.586_601delinsT
ENST00000275493.7:c.2237_2252delinsT MANE Select ENSP00000275493.2:p.Glu746_Thr751delinsVal
ENST00000275493.6:c.2237_2252delinsT ENSP00000275493.2:p.Glu746_Thr751delinsVal
ENST00000442591.5:c.*28+1846_*28+1861delinsT ENSP00000410031.1:n.*28+1846_*28+1861delinsT
ENST00000454757.6:c.2102_2117delinsT ENSP00000395243.3:p.Glu701_Thr706delinsVal
ENST00000455089.5:c.2102_2117delinsT ENSP00000415559.1:p.Glu701_Thr706delinsVal
NM_005228.3:c.2237_2252delinsT , LRG_304t1:c.2237_2252delinsT NP_005219.2:p.Glu746_Thr751delinsVal
NM_001346897.1:c.2102_2117delinsT NP_001333826.1:p.Glu701_Thr706delinsVal
NM_001346898.1:c.2237_2252delinsT NP_001333827.1:p.Glu746_Thr751delinsVal
NM_001346899.1:c.2102_2117delinsT NP_001333828.1:p.Glu701_Thr706delinsVal
NM_001346900.1:c.2078_2093delinsT NP_001333829.1:p.Glu693_Thr698delinsVal
NM_001346941.1:c.1436_1451delinsT NP_001333870.1:p.Glu479_Thr484delinsVal
NM_005228.4:c.2237_2252delinsT NP_005219.2:p.Glu746_Thr751delinsVal
NM_005228.5:c.2237_2252delinsT MANE Select NP_005219.2:p.Glu746_Thr751delinsVal
NM_001346897.2:c.2102_2117delinsT NP_001333826.1:p.Glu701_Thr706delinsVal
NM_001346898.2:c.2237_2252delinsT NP_001333827.1:p.Glu746_Thr751delinsVal
NM_001346900.2:c.2078_2093delinsT NP_001333829.1:p.Glu693_Thr698delinsVal
NM_001346941.2:c.1436_1451delinsT NP_001333870.1:p.Glu479_Thr484delinsVal
NM_001346899.2:c.2102_2117delinsT NP_001333828.1:p.Glu701_Thr706delinsVal