Canonical Allele Identifier: CA454965609

Gene: EGFR

Linked Data

• dbSNP Id: rs2128964495
• MyVariant Identifiers: chr7:g.55259462C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55191769C>G , CM000669.2:g.55191769C>G	GRCh38
NC_000007.13:g.55259462C>G , CM000669.1:g.55259462C>G	GRCh37
NC_000007.12:g.55226956C>G	NCBI36
NG_007726.3:g.177738C>G , LRG_304:g.177738C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000450046.2:c.2361C>G	ENSP00000413354.2:p.Ala787=
ENST00000700145.1:c.869C>G
ENST00000275493.7:c.2520C>G MANE Select	ENSP00000275493.2:p.Ala840=
ENST00000275493.6:c.2520C>G	ENSP00000275493.2:p.Ala840=
ENST00000442591.5:c.*28+18841C>G	ENSP00000410031.1:n.*28+18841C>G
ENST00000454757.6:c.2385C>G	ENSP00000395243.3:p.Ala795=
ENST00000455089.5:c.2385C>G	ENSP00000415559.1:p.Ala795=
NM_005228.3:c.2520C>G , LRG_304t1:c.2520C>G	NP_005219.2:p.Ala840=
NM_001346897.1:c.2385C>G	NP_001333826.1:p.Ala795=
NM_001346898.1:c.2520C>G	NP_001333827.1:p.Ala840=
NM_001346899.1:c.2385C>G	NP_001333828.1:p.Ala795=
NM_001346900.1:c.2361C>G	NP_001333829.1:p.Ala787=
NM_001346941.1:c.1719C>G	NP_001333870.1:p.Ala573=
NM_005228.4:c.2520C>G	NP_005219.2:p.Ala840=
NM_005228.5:c.2520C>G MANE Select	NP_005219.2:p.Ala840=
NM_001346897.2:c.2385C>G	NP_001333826.1:p.Ala795=
NM_001346898.2:c.2520C>G	NP_001333827.1:p.Ala840=
NM_001346900.2:c.2361C>G	NP_001333829.1:p.Ala787=
NM_001346941.2:c.1719C>G	NP_001333870.1:p.Ala573=
NM_001346899.2:c.2385C>G	NP_001333828.1:p.Ala795=