Canonical Allele Identifier: CA645561501

Gene: EGFR

Linked Data

• COSMIC: COSM133189

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174773_55174793del , CM000669.2:g.55174773_55174793del	GRCh38
NC_000007.13:g.55242466_55242486del , CM000669.1:g.55242466_55242486del	GRCh37
NC_000007.12:g.55209960_55209980del	NCBI36
NG_007726.3:g.160742_160762del , LRG_304:g.160742_160762del

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2077_2097del	ENSP00000413354.2:p.Glu693_Ser699del
ENST00000700145.1:c.585_605del
ENST00000275493.7:c.2236_2256del MANE Select	ENSP00000275493.2:p.Glu746_Ser752del
ENST00000275493.6:c.2236_2256del	ENSP00000275493.2:p.Glu746_Ser752del
ENST00000442591.5:c.*28+1845_*28+1865del	ENSP00000410031.1:n.*28+1845_*28+1865del
ENST00000454757.6:c.2101_2121del	ENSP00000395243.3:p.Glu701_Ser707del
ENST00000455089.5:c.2101_2121del	ENSP00000415559.1:p.Glu701_Ser707del
NM_005228.3:c.2236_2256del , LRG_304t1:c.2236_2256del	NP_005219.2:p.Glu746_Ser752del
NM_001346897.1:c.2101_2121del	NP_001333826.1:p.Glu701_Ser707del
NM_001346898.1:c.2236_2256del	NP_001333827.1:p.Glu746_Ser752del
NM_001346899.1:c.2101_2121del	NP_001333828.1:p.Glu701_Ser707del
NM_001346900.1:c.2077_2097del	NP_001333829.1:p.Glu693_Ser699del
NM_001346941.1:c.1435_1455del	NP_001333870.1:p.Glu479_Ser485del
NM_005228.4:c.2236_2256del	NP_005219.2:p.Glu746_Ser752del
NM_005228.5:c.2236_2256del MANE Select	NP_005219.2:p.Glu746_Ser752del
NM_001346897.2:c.2101_2121del	NP_001333826.1:p.Glu701_Ser707del
NM_001346898.2:c.2236_2256del	NP_001333827.1:p.Glu746_Ser752del
NM_001346900.2:c.2077_2097del	NP_001333829.1:p.Glu693_Ser699del
NM_001346941.2:c.1435_1455del	NP_001333870.1:p.Glu479_Ser485del
NM_001346899.2:c.2101_2121del	NP_001333828.1:p.Glu701_Ser707del