Canonical Allele Identifier: CA645561537
Gene: EGFR HGNC NCBI

Linked Data

dbSNP Id: rs2128954823
COSMIC: COSM26718

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174787_55174801del , CM000669.2:g.55174787_55174801del GRCh38
NC_000007.13:g.55242480_55242494del , CM000669.1:g.55242480_55242494del GRCh37
NC_000007.12:g.55209974_55209988del NCBI36
NG_007726.3:g.160756_160770del , LRG_304:g.160756_160770del

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2091_2105del ENSP00000413354.2:p.Thr698_Ala702del
ENST00000700145.1:c.599_613del
ENST00000275493.7:c.2250_2264del MANE Select ENSP00000275493.2:p.Thr751_Ala755del
ENST00000275493.6:c.2250_2264del ENSP00000275493.2:p.Thr751_Ala755del
ENST00000442591.5:c.*28+1859_*28+1873del ENSP00000410031.1:n.*28+1859_*28+1873del
ENST00000454757.6:c.2115_2129del ENSP00000395243.3:p.Thr706_Ala710del
ENST00000455089.5:c.2115_2129del ENSP00000415559.1:p.Thr706_Ala710del
NM_005228.3:c.2250_2264del , LRG_304t1:c.2250_2264del NP_005219.2:p.Thr751_Ala755del
NM_001346897.1:c.2115_2129del NP_001333826.1:p.Thr706_Ala710del
NM_001346898.1:c.2250_2264del NP_001333827.1:p.Thr751_Ala755del
NM_001346899.1:c.2115_2129del NP_001333828.1:p.Thr706_Ala710del
NM_001346900.1:c.2091_2105del NP_001333829.1:p.Thr698_Ala702del
NM_001346941.1:c.1449_1463del NP_001333870.1:p.Thr484_Ala488del
NM_005228.4:c.2250_2264del NP_005219.2:p.Thr751_Ala755del
NM_005228.5:c.2250_2264del MANE Select NP_005219.2:p.Thr751_Ala755del
NM_001346897.2:c.2115_2129del NP_001333826.1:p.Thr706_Ala710del
NM_001346898.2:c.2250_2264del NP_001333827.1:p.Thr751_Ala755del
NM_001346900.2:c.2091_2105del NP_001333829.1:p.Thr698_Ala702del
NM_001346941.2:c.1449_1463del NP_001333870.1:p.Thr484_Ala488del
NM_001346899.2:c.2115_2129del NP_001333828.1:p.Thr706_Ala710del