Canonical Allele Identifier: CA645561546
Gene: EGFR HGNC NCBI

Linked Data

COSMIC: COSM96856

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174789_55174813delinsA , CM000669.2:g.55174789_55174813delinsA GRCh38
NC_000007.13:g.55242482_55242506delinsA , CM000669.1:g.55242482_55242506delinsA GRCh37
NC_000007.12:g.55209976_55210000delinsA NCBI36
NG_007726.3:g.160758_160782delinsA , LRG_304:g.160758_160782delinsA

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2093_2117delinsA ENSP00000413354.2:p.Thr698_Ile706delinsAs...
ENST00000700145.1:c.601_625delinsA
ENST00000275493.7:c.2252_2276delinsA MANE Select ENSP00000275493.2:p.Thr751_Ile759delinsAs...
ENST00000275493.6:c.2252_2276delinsA ENSP00000275493.2:p.Thr751_Ile759delinsAs...
ENST00000442591.5:c.*28+1861_*28+1885delinsA ENSP00000410031.1:n.*28+1861_*28+1885deli...
ENST00000454757.6:c.2117_2141delinsA ENSP00000395243.3:p.Thr706_Ile714delinsAs...
ENST00000455089.5:c.2117_2141delinsA ENSP00000415559.1:p.Thr706_Ile714delinsAs...
NM_005228.3:c.2252_2276delinsA , LRG_304t1:c.2252_2276delinsA NP_005219.2:p.Thr751_Ile759delinsAsn
NM_001346897.1:c.2117_2141delinsA NP_001333826.1:p.Thr706_Ile714delinsAsn
NM_001346898.1:c.2252_2276delinsA NP_001333827.1:p.Thr751_Ile759delinsAsn
NM_001346899.1:c.2117_2141delinsA NP_001333828.1:p.Thr706_Ile714delinsAsn
NM_001346900.1:c.2093_2117delinsA NP_001333829.1:p.Thr698_Ile706delinsAsn
NM_001346941.1:c.1451_1475delinsA NP_001333870.1:p.Thr484_Ile492delinsAsn
NM_005228.4:c.2252_2276delinsA NP_005219.2:p.Thr751_Ile759delinsAsn
NM_005228.5:c.2252_2276delinsA MANE Select NP_005219.2:p.Thr751_Ile759delinsAsn
NM_001346897.2:c.2117_2141delinsA NP_001333826.1:p.Thr706_Ile714delinsAsn
NM_001346898.2:c.2252_2276delinsA NP_001333827.1:p.Thr751_Ile759delinsAsn
NM_001346900.2:c.2093_2117delinsA NP_001333829.1:p.Thr698_Ile706delinsAsn
NM_001346941.2:c.1451_1475delinsA NP_001333870.1:p.Thr484_Ile492delinsAsn
NM_001346899.2:c.2117_2141delinsA NP_001333828.1:p.Thr706_Ile714delinsAsn