Canonical Allele Identifier: CA180527

Gene: EGFR

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174790_55174813del , CM000669.2:g.55174790_55174813del	GRCh38
NC_000007.13:g.55242483_55242506del , CM000669.1:g.55242483_55242506del	GRCh37
NC_000007.12:g.55209977_55210000del	NCBI36
NG_007726.3:g.160759_160782del , LRG_304:g.160759_160782del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2094_2117del	ENSP00000413354.2:p.Ser699_Ile706del
ENST00000700145.1:c.602_625del
ENST00000275493.7:c.2253_2276del MANE Select	ENSP00000275493.2:p.Ser752_Ile759del
ENST00000275493.6:c.2253_2276del	ENSP00000275493.2:p.Ser752_Ile759del
ENST00000442591.5:c.*28+1862_*28+1885del	ENSP00000410031.1:n.*28+1862_*28+1885del
ENST00000454757.6:c.2118_2141del	ENSP00000395243.3:p.Ser707_Ile714del
ENST00000455089.5:c.2118_2141del	ENSP00000415559.1:p.Ser707_Ile714del
NM_005228.3:c.2253_2276del , LRG_304t1:c.2253_2276del	NP_005219.2:p.Ser752_Ile759del
NM_001346897.1:c.2118_2141del	NP_001333826.1:p.Ser707_Ile714del
NM_001346898.1:c.2253_2276del	NP_001333827.1:p.Ser752_Ile759del
NM_001346899.1:c.2118_2141del	NP_001333828.1:p.Ser707_Ile714del
NM_001346900.1:c.2094_2117del	NP_001333829.1:p.Ser699_Ile706del
NM_001346941.1:c.1452_1475del	NP_001333870.1:p.Ser485_Ile492del
NM_005228.4:c.2253_2276del	NP_005219.2:p.Ser752_Ile759del
NM_005228.5:c.2253_2276del MANE Select	NP_005219.2:p.Ser752_Ile759del
NM_001346897.2:c.2118_2141del	NP_001333826.1:p.Ser707_Ile714del
NM_001346898.2:c.2253_2276del	NP_001333827.1:p.Ser752_Ile759del
NM_001346900.2:c.2094_2117del	NP_001333829.1:p.Ser699_Ile706del
NM_001346941.2:c.1452_1475del	NP_001333870.1:p.Ser485_Ile492del
NM_001346899.2:c.2118_2141del	NP_001333828.1:p.Ser707_Ile714del