Canonical Allele Identifier: CA645561502
Gene: EGFR HGNC NCBI

Linked Data

dbSNP Id: rs2128954735
COSMIC: COSM26513

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174773_55174788delinsT , CM000669.2:g.55174773_55174788delinsT GRCh38
NC_000007.13:g.55242466_55242481delinsT , CM000669.1:g.55242466_55242481delinsT GRCh37
NC_000007.12:g.55209960_55209975delinsT NCBI36
NG_007726.3:g.160742_160757delinsT , LRG_304:g.160742_160757delinsT

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2077_2092delinsT ENSP00000413354.2:p.Glu693_Thr698delinsSe...
ENST00000700145.1:c.585_600delinsT
ENST00000275493.7:c.2236_2251delinsT MANE Select ENSP00000275493.2:p.Glu746_Thr751delinsSe...
ENST00000275493.6:c.2236_2251delinsT ENSP00000275493.2:p.Glu746_Thr751delinsSe...
ENST00000442591.5:c.*28+1845_*28+1860delinsT ENSP00000410031.1:n.*28+1845_*28+1860deli...
ENST00000454757.6:c.2101_2116delinsT ENSP00000395243.3:p.Glu701_Thr706delinsSe...
ENST00000455089.5:c.2101_2116delinsT ENSP00000415559.1:p.Glu701_Thr706delinsSe...
NM_005228.3:c.2236_2251delinsT , LRG_304t1:c.2236_2251delinsT NP_005219.2:p.Glu746_Thr751delinsSer
NM_001346897.1:c.2101_2116delinsT NP_001333826.1:p.Glu701_Thr706delinsSer
NM_001346898.1:c.2236_2251delinsT NP_001333827.1:p.Glu746_Thr751delinsSer
NM_001346899.1:c.2101_2116delinsT NP_001333828.1:p.Glu701_Thr706delinsSer
NM_001346900.1:c.2077_2092delinsT NP_001333829.1:p.Glu693_Thr698delinsSer
NM_001346941.1:c.1435_1450delinsT NP_001333870.1:p.Glu479_Thr484delinsSer
NM_005228.4:c.2236_2251delinsT NP_005219.2:p.Glu746_Thr751delinsSer
NM_005228.5:c.2236_2251delinsT MANE Select NP_005219.2:p.Glu746_Thr751delinsSer
NM_001346897.2:c.2101_2116delinsT NP_001333826.1:p.Glu701_Thr706delinsSer
NM_001346898.2:c.2236_2251delinsT NP_001333827.1:p.Glu746_Thr751delinsSer
NM_001346900.2:c.2077_2092delinsT NP_001333829.1:p.Glu693_Thr698delinsSer
NM_001346941.2:c.1435_1450delinsT NP_001333870.1:p.Glu479_Thr484delinsSer
NM_001346899.2:c.2101_2116delinsT NP_001333828.1:p.Glu701_Thr706delinsSer