Canonical Allele Identifier: CA645561504
Gene: EGFR HGNC NCBI

Linked Data

dbSNP Id: rs2128954743
COSMIC: COSM133191

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174773_55174794delinsATCT , CM000669.2:g.55174773_55174794delinsATCT GRCh38
NC_000007.13:g.55242466_55242487delinsATCT , CM000669.1:g.55242466_55242487delinsATCT GRCh37
NC_000007.12:g.55209960_55209981delinsATCT NCBI36
NG_007726.3:g.160742_160763delinsATCT , LRG_304:g.160742_160763delinsATCT

Transcript Alleles

HGVS Amino-acid change
ENST00000450046.2:c.2077_2098delinsATCT ENSP00000413354.2:p.Glu693_Pro700delinsIl...
ENST00000700145.1:c.585_606delinsATCT
ENST00000275493.7:c.2236_2257delinsATCT MANE Select ENSP00000275493.2:p.Glu746_Pro753delinsIl...
ENST00000275493.6:c.2236_2257delinsATCT ENSP00000275493.2:p.Glu746_Pro753delinsIl...
ENST00000442591.5:c.*28+1845_*28+1866delinsATCT ENSP00000410031.1:n.*28+1845_*28+1866deli...
ENST00000454757.6:c.2101_2122delinsATCT ENSP00000395243.3:p.Glu701_Pro708delinsIl...
ENST00000455089.5:c.2101_2122delinsATCT ENSP00000415559.1:p.Glu701_Pro708delinsIl...
NM_005228.3:c.2236_2257delinsATCT , LRG_304t1:c.2236_2257delinsATCT NP_005219.2:p.Glu746_Pro753delinsIleSer
NM_001346897.1:c.2101_2122delinsATCT NP_001333826.1:p.Glu701_Pro708delinsIleSe...
NM_001346898.1:c.2236_2257delinsATCT NP_001333827.1:p.Glu746_Pro753delinsIleSe...
NM_001346899.1:c.2101_2122delinsATCT NP_001333828.1:p.Glu701_Pro708delinsIleSe...
NM_001346900.1:c.2077_2098delinsATCT NP_001333829.1:p.Glu693_Pro700delinsIleSe...
NM_001346941.1:c.1435_1456delinsATCT NP_001333870.1:p.Glu479_Pro486delinsIleSe...
NM_005228.4:c.2236_2257delinsATCT NP_005219.2:p.Glu746_Pro753delinsIleSer
NM_005228.5:c.2236_2257delinsATCT MANE Select NP_005219.2:p.Glu746_Pro753delinsIleSer
NM_001346897.2:c.2101_2122delinsATCT NP_001333826.1:p.Glu701_Pro708delinsIleSe...
NM_001346898.2:c.2236_2257delinsATCT NP_001333827.1:p.Glu746_Pro753delinsIleSe...
NM_001346900.2:c.2077_2098delinsATCT NP_001333829.1:p.Glu693_Pro700delinsIleSe...
NM_001346941.2:c.1435_1456delinsATCT NP_001333870.1:p.Glu479_Pro486delinsIleSe...
NM_001346899.2:c.2101_2122delinsATCT NP_001333828.1:p.Glu701_Pro708delinsIleSe...