Canonical Allele Identifier: CA367580182

Gene: EGFR

Linked Data

• dbSNP Id: rs2128964513
• COSMIC: COSM133206
• MyVariant Identifiers: chr7:g.55259472C>G (hg19) ; chr7:g.55191779C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55191779C>G , CM000669.2:g.55191779C>G	GRCh38
NC_000007.13:g.55259472C>G , CM000669.1:g.55259472C>G	GRCh37
NC_000007.12:g.55226966C>G	NCBI36
NG_007726.3:g.177748C>G , LRG_304:g.177748C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2371C>G	ENSP00000413354.2:p.Leu791Val
ENST00000700145.1:c.879C>G
ENST00000275493.7:c.2530C>G MANE Select	ENSP00000275493.2:p.Leu844Val
ENST00000275493.6:c.2530C>G	ENSP00000275493.2:p.Leu844Val
ENST00000442591.5:c.*28+18851C>G	ENSP00000410031.1:n.*28+18851C>G
ENST00000454757.6:c.2395C>G	ENSP00000395243.3:p.Leu799Val
ENST00000455089.5:c.2395C>G	ENSP00000415559.1:p.Leu799Val
NM_005228.3:c.2530C>G , LRG_304t1:c.2530C>G	NP_005219.2:p.Leu844Val
NM_001346897.1:c.2395C>G	NP_001333826.1:p.Leu799Val
NM_001346898.1:c.2530C>G	NP_001333827.1:p.Leu844Val
NM_001346899.1:c.2395C>G	NP_001333828.1:p.Leu799Val
NM_001346900.1:c.2371C>G	NP_001333829.1:p.Leu791Val
NM_001346941.1:c.1729C>G	NP_001333870.1:p.Leu577Val
NM_005228.4:c.2530C>G	NP_005219.2:p.Leu844Val
NM_005228.5:c.2530C>G MANE Select	NP_005219.2:p.Leu844Val
NM_001346897.2:c.2395C>G	NP_001333826.1:p.Leu799Val
NM_001346898.2:c.2530C>G	NP_001333827.1:p.Leu844Val
NM_001346900.2:c.2371C>G	NP_001333829.1:p.Leu791Val
NM_001346941.2:c.1729C>G	NP_001333870.1:p.Leu577Val
NM_001346899.2:c.2395C>G	NP_001333828.1:p.Leu799Val