Canonical Allele Identifier: CA454979611

Gene: EGFR

Linked Data

• dbSNP Id: rs727503017
• MyVariant Identifiers: chr7:g.55242495C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55174802C>A , CM000669.2:g.55174802C>A	GRCh38
NC_000007.13:g.55242495C>A , CM000669.1:g.55242495C>A	GRCh37
NC_000007.12:g.55209989C>A	NCBI36
NG_007726.3:g.160771C>A , LRG_304:g.160771C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2106C>A	ENSP00000413354.2:p.Ala702=
ENST00000700145.1:c.614C>A
ENST00000275493.7:c.2265C>A MANE Select	ENSP00000275493.2:p.Ala755=
ENST00000275493.6:c.2265C>A	ENSP00000275493.2:p.Ala755=
ENST00000442591.5:c.*28+1874C>A	ENSP00000410031.1:n.*28+1874C>A
ENST00000454757.6:c.2130C>A	ENSP00000395243.3:p.Ala710=
ENST00000455089.5:c.2130C>A	ENSP00000415559.1:p.Ala710=
NM_005228.3:c.2265C>A , LRG_304t1:c.2265C>A	NP_005219.2:p.Ala755=
NM_001346897.1:c.2130C>A	NP_001333826.1:p.Ala710=
NM_001346898.1:c.2265C>A	NP_001333827.1:p.Ala755=
NM_001346899.1:c.2130C>A	NP_001333828.1:p.Ala710=
NM_001346900.1:c.2106C>A	NP_001333829.1:p.Ala702=
NM_001346941.1:c.1464C>A	NP_001333870.1:p.Ala488=
NM_005228.4:c.2265C>A	NP_005219.2:p.Ala755=
NM_005228.5:c.2265C>A MANE Select	NP_005219.2:p.Ala755=
NM_001346897.2:c.2130C>A	NP_001333826.1:p.Ala710=
NM_001346898.2:c.2265C>A	NP_001333827.1:p.Ala755=
NM_001346900.2:c.2106C>A	NP_001333829.1:p.Ala702=
NM_001346941.2:c.1464C>A	NP_001333870.1:p.Ala488=
NM_001346899.2:c.2130C>A	NP_001333828.1:p.Ala710=