Canonical Allele Identifier: CA180594

Gene: EGFR

Linked Data

• ClinVar Variation Id: 177663
• ClinVar RCV Id: RCV000154252
• dbSNP Id: rs727504266
• MyVariant Identifiers: chr7:g.55242465_55242473del (hg19) ; chr7:g.55174772_55174780del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174772_55174780del , CM000669.2:g.55174772_55174780del	GRCh38
NC_000007.13:g.55242465_55242473del , CM000669.1:g.55242465_55242473del	GRCh37
NC_000007.12:g.55209959_55209967del	NCBI36
NG_007726.3:g.160741_160749del , LRG_304:g.160741_160749del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2076_2084del	ENSP00000413354.2:p.Glu693_Arg695del
ENST00000700145.1:c.584_592del
ENST00000275493.7:c.2235_2243del MANE Select	ENSP00000275493.2:p.Glu746_Arg748del
ENST00000275493.6:c.2235_2243del	ENSP00000275493.2:p.Glu746_Arg748del
ENST00000442591.5:c.*28+1844_*28+1852del	ENSP00000410031.1:n.*28+1844_*28+1852del
ENST00000454757.6:c.2100_2108del	ENSP00000395243.3:p.Glu701_Arg703del
ENST00000455089.5:c.2100_2108del	ENSP00000415559.1:p.Glu701_Arg703del
NM_005228.3:c.2235_2243del , LRG_304t1:c.2235_2243del	NP_005219.2:p.Glu746_Arg748del
NM_001346897.1:c.2100_2108del	NP_001333826.1:p.Glu701_Arg703del
NM_001346898.1:c.2235_2243del	NP_001333827.1:p.Glu746_Arg748del
NM_001346899.1:c.2100_2108del	NP_001333828.1:p.Glu701_Arg703del
NM_001346900.1:c.2076_2084del	NP_001333829.1:p.Glu693_Arg695del
NM_001346941.1:c.1434_1442del	NP_001333870.1:p.Glu479_Arg481del
NM_005228.4:c.2235_2243del	NP_005219.2:p.Glu746_Arg748del
NM_005228.5:c.2235_2243del MANE Select	NP_005219.2:p.Glu746_Arg748del
NM_001346897.2:c.2100_2108del	NP_001333826.1:p.Glu701_Arg703del
NM_001346898.2:c.2235_2243del	NP_001333827.1:p.Glu746_Arg748del
NM_001346900.2:c.2076_2084del	NP_001333829.1:p.Glu693_Arg695del
NM_001346941.2:c.1434_1442del	NP_001333870.1:p.Glu479_Arg481del
NM_001346899.2:c.2100_2108del	NP_001333828.1:p.Glu701_Arg703del