Canonical Allele Identifier: CA645561496
Gene: EGFR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174773_55174794delinsCTCT , CM000669.2:g.55174773_55174794delinsCTCT GRCh38
NC_000007.13:g.55242466_55242487delinsCTCT , CM000669.1:g.55242466_55242487delinsCTCT GRCh37
NC_000007.12:g.55209960_55209981delinsCTCT NCBI36
NG_007726.3:g.160742_160763delinsCTCT , LRG_304:g.160742_160763delinsCTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000450046.2:c.2077_2098delinsCTCT ENSP00000413354.2:p.Glu693_Pro700delinsLeuSer
ENST00000700145.1:c.585_606delinsCTCT
ENST00000275493.7:c.2236_2257delinsCTCT MANE Select ENSP00000275493.2:p.Glu746_Pro753delinsLeuSer
ENST00000275493.6:c.2236_2257delinsCTCT ENSP00000275493.2:p.Glu746_Pro753delinsLeuSer
ENST00000442591.5:c.*28+1845_*28+1866delinsCTCT ENSP00000410031.1:n.*28+1845_*28+1866delinsCTCT
ENST00000454757.6:c.2101_2122delinsCTCT ENSP00000395243.3:p.Glu701_Pro708delinsLeuSer
ENST00000455089.5:c.2101_2122delinsCTCT ENSP00000415559.1:p.Glu701_Pro708delinsLeuSer
NM_005228.3:c.2236_2257delinsCTCT , LRG_304t1:c.2236_2257delinsCTCT NP_005219.2:p.Glu746_Pro753delinsLeuSer
NM_001346897.1:c.2101_2122delinsCTCT NP_001333826.1:p.Glu701_Pro708delinsLeuSer
NM_001346898.1:c.2236_2257delinsCTCT NP_001333827.1:p.Glu746_Pro753delinsLeuSer
NM_001346899.1:c.2101_2122delinsCTCT NP_001333828.1:p.Glu701_Pro708delinsLeuSer
NM_001346900.1:c.2077_2098delinsCTCT NP_001333829.1:p.Glu693_Pro700delinsLeuSer
NM_001346941.1:c.1435_1456delinsCTCT NP_001333870.1:p.Glu479_Pro486delinsLeuSer
NM_005228.4:c.2236_2257delinsCTCT NP_005219.2:p.Glu746_Pro753delinsLeuSer
NM_005228.5:c.2236_2257delinsCTCT MANE Select NP_005219.2:p.Glu746_Pro753delinsLeuSer
NM_001346897.2:c.2101_2122delinsCTCT NP_001333826.1:p.Glu701_Pro708delinsLeuSer
NM_001346898.2:c.2236_2257delinsCTCT NP_001333827.1:p.Glu746_Pro753delinsLeuSer
NM_001346900.2:c.2077_2098delinsCTCT NP_001333829.1:p.Glu693_Pro700delinsLeuSer
NM_001346941.2:c.1435_1456delinsCTCT NP_001333870.1:p.Glu479_Pro486delinsLeuSer
NM_001346899.2:c.2101_2122delinsCTCT NP_001333828.1:p.Glu701_Pro708delinsLeuSer
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