Canonical Allele Identifier: CA645561519

Gene: EGFR

Linked Data

• COSMIC: COSM255211

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174775_55174795del , CM000669.2:g.55174775_55174795del	GRCh38
NC_000007.13:g.55242468_55242488del , CM000669.1:g.55242468_55242488del	GRCh37
NC_000007.12:g.55209962_55209982del	NCBI36
NG_007726.3:g.160744_160764del , LRG_304:g.160744_160764del

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2079_2099del	ENSP00000413354.2:p.Leu694_Pro700del
ENST00000700145.1:c.587_607del
ENST00000275493.7:c.2238_2258del MANE Select	ENSP00000275493.2:p.Leu747_Pro753del
ENST00000275493.6:c.2238_2258del	ENSP00000275493.2:p.Leu747_Pro753del
ENST00000442591.5:c.*28+1847_*28+1867del	ENSP00000410031.1:n.*28+1847_*28+1867del
ENST00000454757.6:c.2103_2123del	ENSP00000395243.3:p.Leu702_Pro708del
ENST00000455089.5:c.2103_2123del	ENSP00000415559.1:p.Leu702_Pro708del
NM_005228.3:c.2238_2258del , LRG_304t1:c.2238_2258del	NP_005219.2:p.Leu747_Pro753del
NM_001346897.1:c.2103_2123del	NP_001333826.1:p.Leu702_Pro708del
NM_001346898.1:c.2238_2258del	NP_001333827.1:p.Leu747_Pro753del
NM_001346899.1:c.2103_2123del	NP_001333828.1:p.Leu702_Pro708del
NM_001346900.1:c.2079_2099del	NP_001333829.1:p.Leu694_Pro700del
NM_001346941.1:c.1437_1457del	NP_001333870.1:p.Leu480_Pro486del
NM_005228.4:c.2238_2258del	NP_005219.2:p.Leu747_Pro753del
NM_005228.5:c.2238_2258del MANE Select	NP_005219.2:p.Leu747_Pro753del
NM_001346897.2:c.2103_2123del	NP_001333826.1:p.Leu702_Pro708del
NM_001346898.2:c.2238_2258del	NP_001333827.1:p.Leu747_Pro753del
NM_001346900.2:c.2079_2099del	NP_001333829.1:p.Leu694_Pro700del
NM_001346941.2:c.1437_1457del	NP_001333870.1:p.Leu480_Pro486del
NM_001346899.2:c.2103_2123del	NP_001333828.1:p.Leu702_Pro708del