Canonical Allele Identifier: CA645561544

Gene: EGFR

Linked Data

• COSMIC: COSM133200

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174788_55174813delinsTC , CM000669.2:g.55174788_55174813delinsTC	GRCh38
NC_000007.13:g.55242481_55242506delinsTC , CM000669.1:g.55242481_55242506delinsTC	GRCh37
NC_000007.12:g.55209975_55210000delinsTC	NCBI36
NG_007726.3:g.160757_160782delinsTC , LRG_304:g.160757_160782delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2092_2117delinsTC	ENSP00000413354.2:p.Thr698_Ile706delinsSe...
ENST00000700145.1:c.600_625delinsTC
ENST00000275493.7:c.2251_2276delinsTC MANE Select	ENSP00000275493.2:p.Thr751_Ile759delinsSe...
ENST00000275493.6:c.2251_2276delinsTC	ENSP00000275493.2:p.Thr751_Ile759delinsSe...
ENST00000442591.5:c.*28+1860_*28+1885delinsTC	ENSP00000410031.1:n.*28+1860_*28+1885deli...
ENST00000454757.6:c.2116_2141delinsTC	ENSP00000395243.3:p.Thr706_Ile714delinsSe...
ENST00000455089.5:c.2116_2141delinsTC	ENSP00000415559.1:p.Thr706_Ile714delinsSe...
NM_005228.3:c.2251_2276delinsTC , LRG_304t1:c.2251_2276delinsTC	NP_005219.2:p.Thr751_Ile759delinsSer
NM_001346897.1:c.2116_2141delinsTC	NP_001333826.1:p.Thr706_Ile714delinsSer
NM_001346898.1:c.2251_2276delinsTC	NP_001333827.1:p.Thr751_Ile759delinsSer
NM_001346899.1:c.2116_2141delinsTC	NP_001333828.1:p.Thr706_Ile714delinsSer
NM_001346900.1:c.2092_2117delinsTC	NP_001333829.1:p.Thr698_Ile706delinsSer
NM_001346941.1:c.1450_1475delinsTC	NP_001333870.1:p.Thr484_Ile492delinsSer
NM_005228.4:c.2251_2276delinsTC	NP_005219.2:p.Thr751_Ile759delinsSer
NM_005228.5:c.2251_2276delinsTC MANE Select	NP_005219.2:p.Thr751_Ile759delinsSer
NM_001346897.2:c.2116_2141delinsTC	NP_001333826.1:p.Thr706_Ile714delinsSer
NM_001346898.2:c.2251_2276delinsTC	NP_001333827.1:p.Thr751_Ile759delinsSer
NM_001346900.2:c.2092_2117delinsTC	NP_001333829.1:p.Thr698_Ile706delinsSer
NM_001346941.2:c.1450_1475delinsTC	NP_001333870.1:p.Thr484_Ile492delinsSer
NM_001346899.2:c.2116_2141delinsTC	NP_001333828.1:p.Thr706_Ile714delinsSer