Canonical Allele Identifier: CA135772

Gene: EGFR

Linked Data

• ClinVar Variation Id: 45224
• ClinVar RCV Id: RCV000038379 ; RCV000114405
• dbSNP Id: rs28929495
• MyVariant Identifiers: chr7:g.55241707G>C (hg19) ; chr7:g.55174014G>C (hg38)
• PubMed: PMID:15118073 ; PMID:15118125 ; PMID:15788655 ; PMID:24712396

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174014G>C , CM000669.2:g.55174014G>C	GRCh38
NC_000007.13:g.55241707G>C , CM000669.1:g.55241707G>C	GRCh37
NC_000007.12:g.55209201G>C	NCBI36
NG_007726.3:g.159983G>C , LRG_304:g.159983G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.1996G>C	ENSP00000413354.2:p.Gly666Arg
ENST00000700145.1:c.504G>C
ENST00000275493.7:c.2155G>C MANE Select	ENSP00000275493.2:p.Gly719Arg
ENST00000275493.6:c.2155G>C	ENSP00000275493.2:p.Gly719Arg
ENST00000442591.5:c.*28+1086G>C	ENSP00000410031.1:n.*28+1086G>C
ENST00000454757.6:c.2020G>C	ENSP00000395243.3:p.Gly674Arg
ENST00000455089.5:c.2020G>C	ENSP00000415559.1:p.Gly674Arg
NM_005228.3:c.2155G>C , LRG_304t1:c.2155G>C	NP_005219.2:p.Gly719Arg
NM_001346897.1:c.2020G>C	NP_001333826.1:p.Gly674Arg
NM_001346898.1:c.2155G>C	NP_001333827.1:p.Gly719Arg
NM_001346899.1:c.2020G>C	NP_001333828.1:p.Gly674Arg
NM_001346900.1:c.1996G>C	NP_001333829.1:p.Gly666Arg
NM_001346941.1:c.1354G>C	NP_001333870.1:p.Gly452Arg
NM_005228.4:c.2155G>C	NP_005219.2:p.Gly719Arg
NM_005228.5:c.2155G>C MANE Select	NP_005219.2:p.Gly719Arg
NM_001346897.2:c.2020G>C	NP_001333826.1:p.Gly674Arg
NM_001346898.2:c.2155G>C	NP_001333827.1:p.Gly719Arg
NM_001346900.2:c.1996G>C	NP_001333829.1:p.Gly666Arg
NM_001346941.2:c.1354G>C	NP_001333870.1:p.Gly452Arg
NM_001346899.2:c.2020G>C	NP_001333828.1:p.Gly674Arg