Canonical Allele Identifier: CA645561530
Gene: EGFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174776_55174789delinsCA , CM000669.2:g.55174776_55174789delinsCA GRCh38
NC_000007.13:g.55242469_55242482delinsCA , CM000669.1:g.55242469_55242482delinsCA GRCh37
NC_000007.12:g.55209963_55209976delinsCA NCBI36
NG_007726.3:g.160745_160758delinsCA , LRG_304:g.160745_160758delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000450046.2:c.2080_2093delinsCA ENSP00000413354.2:p.Leu694_Thr698delinsGln
ENST00000700145.1:c.588_601delinsCA
ENST00000275493.7:c.2239_2252delinsCA MANE Select ENSP00000275493.2:p.Leu747_Thr751delinsGln
ENST00000275493.6:c.2239_2252delinsCA ENSP00000275493.2:p.Leu747_Thr751delinsGln
ENST00000442591.5:c.*28+1848_*28+1861delinsCA ENSP00000410031.1:n.*28+1848_*28+1861delinsCA
ENST00000454757.6:c.2104_2117delinsCA ENSP00000395243.3:p.Leu702_Thr706delinsGln
ENST00000455089.5:c.2104_2117delinsCA ENSP00000415559.1:p.Leu702_Thr706delinsGln
NM_005228.3:c.2239_2252delinsCA , LRG_304t1:c.2239_2252delinsCA NP_005219.2:p.Leu747_Thr751delinsGln
NM_001346897.1:c.2104_2117delinsCA NP_001333826.1:p.Leu702_Thr706delinsGln
NM_001346898.1:c.2239_2252delinsCA NP_001333827.1:p.Leu747_Thr751delinsGln
NM_001346899.1:c.2104_2117delinsCA NP_001333828.1:p.Leu702_Thr706delinsGln
NM_001346900.1:c.2080_2093delinsCA NP_001333829.1:p.Leu694_Thr698delinsGln
NM_001346941.1:c.1438_1451delinsCA NP_001333870.1:p.Leu480_Thr484delinsGln
NM_005228.4:c.2239_2252delinsCA NP_005219.2:p.Leu747_Thr751delinsGln
NM_005228.5:c.2239_2252delinsCA MANE Select NP_005219.2:p.Leu747_Thr751delinsGln
NM_001346897.2:c.2104_2117delinsCA NP_001333826.1:p.Leu702_Thr706delinsGln
NM_001346898.2:c.2239_2252delinsCA NP_001333827.1:p.Leu747_Thr751delinsGln
NM_001346900.2:c.2080_2093delinsCA NP_001333829.1:p.Leu694_Thr698delinsGln
NM_001346941.2:c.1438_1451delinsCA NP_001333870.1:p.Leu480_Thr484delinsGln
NM_001346899.2:c.2104_2117delinsCA NP_001333828.1:p.Leu702_Thr706delinsGln