Canonical Allele Identifier: CA1708918334
Gene: EGFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174775_55174794delinsATTAAGAGAAGCAACATCTC , CM000669.2:g.55174775_55174794delinsATTAAGAGAAGCAACATCTC GRCh38
NC_000007.13:g.55242468_55242487delinsATTAAGAGAAGCAACATCTC , CM000669.1:g.55242468_55242487delinsATTAAGAGAAGCAACATCTC GRCh37
NC_000007.12:g.55209962_55209981delinsATTAAGAGAAGCAACATCTC NCBI36
NG_007726.3:g.160744_160763delinsATTAAGAGAAGCAACATCTC , LRG_304:g.160744_160763delinsATTAAGAGAAGCAACATCTC

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2079_2098delinsATTAAGAGAAGCAACATCTC ENSP00000413354.2:p.Glu693=
ENST00000700145.1:c.587_606delinsATTAAGAGAAGCAACATCTC
ENST00000275493.7:c.2238_2257delinsATTAAGAGAAGCAACATCTC MANE Select ENSP00000275493.2:p.Glu746=
ENST00000275493.6:c.2238_2257delinsATTAAGAGAAGCAACATCTC ENSP00000275493.2:p.Glu746=
ENST00000442591.5:c.*28+1847_*28+1866delinsATTAAGAGAAGCAACATCTC ENSP00000410031.1:n.*28+1847_*28+1866deli...
ENST00000454757.6:c.2103_2122delinsATTAAGAGAAGCAACATCTC ENSP00000395243.3:p.Glu701=
ENST00000455089.5:c.2103_2122delinsATTAAGAGAAGCAACATCTC ENSP00000415559.1:p.Glu701=
NM_005228.3:c.2238_2257delinsATTAAGAGAAGCAACATCTC , LRG_304t1:c.2238_2257delinsATTAAGAGAAGCAACATCTC NP_005219.2:p.Glu746=
NM_001346897.1:c.2103_2122delinsATTAAGAGAAGCAACATCTC NP_001333826.1:p.Glu701=
NM_001346898.1:c.2238_2257delinsATTAAGAGAAGCAACATCTC NP_001333827.1:p.Glu746=
NM_001346899.1:c.2103_2122delinsATTAAGAGAAGCAACATCTC NP_001333828.1:p.Glu701=
NM_001346900.1:c.2079_2098delinsATTAAGAGAAGCAACATCTC NP_001333829.1:p.Glu693=
NM_001346941.1:c.1437_1456delinsATTAAGAGAAGCAACATCTC NP_001333870.1:p.Glu479=
NM_005228.4:c.2238_2257delinsATTAAGAGAAGCAACATCTC NP_005219.2:p.Glu746=
NM_005228.5:c.2238_2257delinsATTAAGAGAAGCAACATCTC MANE Select NP_005219.2:p.Glu746=
NM_001346897.2:c.2103_2122delinsATTAAGAGAAGCAACATCTC NP_001333826.1:p.Glu701=
NM_001346898.2:c.2238_2257delinsATTAAGAGAAGCAACATCTC NP_001333827.1:p.Glu746=
NM_001346900.2:c.2079_2098delinsATTAAGAGAAGCAACATCTC NP_001333829.1:p.Glu693=
NM_001346941.2:c.1437_1456delinsATTAAGAGAAGCAACATCTC NP_001333870.1:p.Glu479=
NM_001346899.2:c.2103_2122delinsATTAAGAGAAGCAACATCTC NP_001333828.1:p.Glu701=