Canonical Allele Identifier: CA645561566
Gene: EGFR HGNC NCBI
EGFR-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2128958303
COSMIC: COSM12379

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55181316_55181317insTGCGTG , CM000669.2:g.55181316_55181317insTGCGTG GRCh38
NC_000007.13:g.55249009_55249010insTGCGTG , CM000669.1:g.55249009_55249010insTGCGTG GRCh37
NC_000007.12:g.55216503_55216504insTGCGTG NCBI36
NG_007726.3:g.167285_167286insTGCGTG , LRG_304:g.167285_167286insTGCGTG

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2148_2149insTGCGTG (EGFR) ENSP00000413354.2:p.Val716_Asp717insCysVa...
ENST00000700145.1:c.656_657insTGCGTG (EGFR)
ENST00000275493.7:c.2307_2308insTGCGTG (EGFR) MANE Select ENSP00000275493.2:p.Val769_Asp770insCysVa...
ENST00000275493.6:c.2307_2308insTGCGTG (EGFR) ENSP00000275493.2:p.Val769_Asp770insCysVa...
ENST00000442591.5:c.*28+8388_*28+8389insTGCGTG (EGFR) ENSP00000410031.1:n.*28+8388_*28+8389insT...
ENST00000454757.6:c.2172_2173insTGCGTG (EGFR) ENSP00000395243.3:p.Val724_Asp725insCysVa...
ENST00000455089.5:c.2172_2173insTGCGTG (EGFR) ENSP00000415559.1:p.Val724_Asp725insCysVa...
NM_005228.3:c.2307_2308insTGCGTG , LRG_304t1:c.2307_2308insTGCGTG (EGFR) NP_005219.2:p.Val769_Asp770insCysVal
NR_047551.1:n.1259_1260insACACGC (EGFR-AS1)
NM_001346897.1:c.2172_2173insTGCGTG (EGFR) NP_001333826.1:p.Val724_Asp725insCysVal
NM_001346898.1:c.2307_2308insTGCGTG (EGFR) NP_001333827.1:p.Val769_Asp770insCysVal
NM_001346899.1:c.2172_2173insTGCGTG (EGFR) NP_001333828.1:p.Val724_Asp725insCysVal
NM_001346900.1:c.2148_2149insTGCGTG (EGFR) NP_001333829.1:p.Val716_Asp717insCysVal
NM_001346941.1:c.1506_1507insTGCGTG (EGFR) NP_001333870.1:p.Val502_Asp503insCysVal
NM_005228.4:c.2307_2308insTGCGTG (EGFR) NP_005219.2:p.Val769_Asp770insCysVal
NM_005228.5:c.2307_2308insTGCGTG (EGFR) MANE Select NP_005219.2:p.Val769_Asp770insCysVal
NM_001346897.2:c.2172_2173insTGCGTG (EGFR) NP_001333826.1:p.Val724_Asp725insCysVal
NM_001346898.2:c.2307_2308insTGCGTG (EGFR) NP_001333827.1:p.Val769_Asp770insCysVal
NM_001346900.2:c.2148_2149insTGCGTG (EGFR) NP_001333829.1:p.Val716_Asp717insCysVal
NM_001346941.2:c.1506_1507insTGCGTG (EGFR) NP_001333870.1:p.Val502_Asp503insCysVal
NM_001346899.2:c.2172_2173insTGCGTG (EGFR) NP_001333828.1:p.Val724_Asp725insCysVal