Canonical Allele Identifier: CA645561551

Gene: EGFR

Linked Data

• COSMIC: COSM24269

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174795_55174815del , CM000669.2:g.55174795_55174815del	GRCh38
NC_000007.13:g.55242488_55242508del , CM000669.1:g.55242488_55242508del	GRCh37
NC_000007.12:g.55209982_55210002del	NCBI36
NG_007726.3:g.160764_160784del , LRG_304:g.160764_160784del

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2099_2119del	ENSP00000413354.2:p.Pro700_Ile706del
ENST00000700145.1:c.607_627del
ENST00000275493.7:c.2258_2278del MANE Select	ENSP00000275493.2:p.Pro753_Ile759del
ENST00000275493.6:c.2258_2278del	ENSP00000275493.2:p.Pro753_Ile759del
ENST00000442591.5:c.*28+1867_*28+1887del	ENSP00000410031.1:n.*28+1867_*28+1887del
ENST00000454757.6:c.2123_2143del	ENSP00000395243.3:p.Pro708_Ile714del
ENST00000455089.5:c.2123_2143del	ENSP00000415559.1:p.Pro708_Ile714del
NM_005228.3:c.2258_2278del , LRG_304t1:c.2258_2278del	NP_005219.2:p.Pro753_Ile759del
NM_001346897.1:c.2123_2143del	NP_001333826.1:p.Pro708_Ile714del
NM_001346898.1:c.2258_2278del	NP_001333827.1:p.Pro753_Ile759del
NM_001346899.1:c.2123_2143del	NP_001333828.1:p.Pro708_Ile714del
NM_001346900.1:c.2099_2119del	NP_001333829.1:p.Pro700_Ile706del
NM_001346941.1:c.1457_1477del	NP_001333870.1:p.Pro486_Ile492del
NM_005228.4:c.2258_2278del	NP_005219.2:p.Pro753_Ile759del
NM_005228.5:c.2258_2278del MANE Select	NP_005219.2:p.Pro753_Ile759del
NM_001346897.2:c.2123_2143del	NP_001333826.1:p.Pro708_Ile714del
NM_001346898.2:c.2258_2278del	NP_001333827.1:p.Pro753_Ile759del
NM_001346900.2:c.2099_2119del	NP_001333829.1:p.Pro700_Ile706del
NM_001346941.2:c.1457_1477del	NP_001333870.1:p.Pro486_Ile492del
NM_001346899.2:c.2123_2143del	NP_001333828.1:p.Pro708_Ile714del