Canonical Allele Identifier: CA180573
Gene: EGFR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174775_55174788delinsGC , CM000669.2:g.55174775_55174788delinsGC GRCh38
NC_000007.13:g.55242468_55242481delinsGC , CM000669.1:g.55242468_55242481delinsGC GRCh37
NC_000007.12:g.55209962_55209975delinsGC NCBI36
NG_007726.3:g.160744_160757delinsGC , LRG_304:g.160744_160757delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000450046.2:c.2079_2092delinsGC ENSP00000413354.2:p.Leu694_Thr698delinsPro
ENST00000700145.1:c.587_600delinsGC
ENST00000275493.7:c.2238_2251delinsGC MANE Select ENSP00000275493.2:p.Leu747_Thr751delinsPro
ENST00000275493.6:c.2238_2251delinsGC ENSP00000275493.2:p.Leu747_Thr751delinsPro
ENST00000442591.5:c.*28+1847_*28+1860delinsGC ENSP00000410031.1:n.*28+1847_*28+1860delinsGC
ENST00000454757.6:c.2103_2116delinsGC ENSP00000395243.3:p.Leu702_Thr706delinsPro
ENST00000455089.5:c.2103_2116delinsGC ENSP00000415559.1:p.Leu702_Thr706delinsPro
NM_005228.3:c.2238_2251delinsGC , LRG_304t1:c.2238_2251delinsGC NP_005219.2:p.Leu747_Thr751delinsPro
NM_001346897.1:c.2103_2116delinsGC NP_001333826.1:p.Leu702_Thr706delinsPro
NM_001346898.1:c.2238_2251delinsGC NP_001333827.1:p.Leu747_Thr751delinsPro
NM_001346899.1:c.2103_2116delinsGC NP_001333828.1:p.Leu702_Thr706delinsPro
NM_001346900.1:c.2079_2092delinsGC NP_001333829.1:p.Leu694_Thr698delinsPro
NM_001346941.1:c.1437_1450delinsGC NP_001333870.1:p.Leu480_Thr484delinsPro
NM_005228.4:c.2238_2251delinsGC NP_005219.2:p.Leu747_Thr751delinsPro
NM_005228.5:c.2238_2251delinsGC MANE Select NP_005219.2:p.Leu747_Thr751delinsPro
NM_001346897.2:c.2103_2116delinsGC NP_001333826.1:p.Leu702_Thr706delinsPro
NM_001346898.2:c.2238_2251delinsGC NP_001333827.1:p.Leu747_Thr751delinsPro
NM_001346900.2:c.2079_2092delinsGC NP_001333829.1:p.Leu694_Thr698delinsPro
NM_001346941.2:c.1437_1450delinsGC NP_001333870.1:p.Leu480_Thr484delinsPro
NM_001346899.2:c.2103_2116delinsGC NP_001333828.1:p.Leu702_Thr706delinsPro
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