Canonical Allele Identifier: CA367580220

Gene: EGFR

Linked Data

• dbSNP Id: rs2128964554
• COSMIC: COSM4384126
• MyVariant Identifiers: chr7:g.55259490C>G (hg19) ; chr7:g.55191797C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55191797C>G , CM000669.2:g.55191797C>G	GRCh38
NC_000007.13:g.55259490C>G , CM000669.1:g.55259490C>G	GRCh37
NC_000007.12:g.55226984C>G	NCBI36
NG_007726.3:g.177766C>G , LRG_304:g.177766C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2389C>G	ENSP00000413354.2:p.His797Asp
ENST00000700145.1:c.897C>G
ENST00000275493.7:c.2548C>G MANE Select	ENSP00000275493.2:p.His850Asp
ENST00000275493.6:c.2548C>G	ENSP00000275493.2:p.His850Asp
ENST00000442591.5:c.*28+18869C>G	ENSP00000410031.1:n.*28+18869C>G
ENST00000454757.6:c.2413C>G	ENSP00000395243.3:p.His805Asp
ENST00000455089.5:c.2413C>G	ENSP00000415559.1:p.His805Asp
NM_005228.3:c.2548C>G , LRG_304t1:c.2548C>G	NP_005219.2:p.His850Asp
NM_001346897.1:c.2413C>G	NP_001333826.1:p.His805Asp
NM_001346898.1:c.2548C>G	NP_001333827.1:p.His850Asp
NM_001346899.1:c.2413C>G	NP_001333828.1:p.His805Asp
NM_001346900.1:c.2389C>G	NP_001333829.1:p.His797Asp
NM_001346941.1:c.1747C>G	NP_001333870.1:p.His583Asp
NM_005228.4:c.2548C>G	NP_005219.2:p.His850Asp
NM_005228.5:c.2548C>G MANE Select	NP_005219.2:p.His850Asp
NM_001346897.2:c.2413C>G	NP_001333826.1:p.His805Asp
NM_001346898.2:c.2548C>G	NP_001333827.1:p.His850Asp
NM_001346900.2:c.2389C>G	NP_001333829.1:p.His797Asp
NM_001346941.2:c.1747C>G	NP_001333870.1:p.His583Asp
NM_001346899.2:c.2413C>G	NP_001333828.1:p.His805Asp