Canonical Allele Identifier: CA16602541
Gene: EGFR HGNC NCBI

Linked Data

ClinVar Variation Id: 376079
ClinVar RCV Id: RCV000423407
dbSNP Id: rs121913466
COSMIC: COSM13183

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55174762T>C , CM000669.2:g.55174762T>C GRCh38
NC_000007.13:g.55242455T>C , CM000669.1:g.55242455T>C GRCh37
NC_000007.12:g.55209949T>C NCBI36
NG_007726.3:g.160731T>C , LRG_304:g.160731T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000275493.7:c.2225T>C MANE Select ENSP00000275493.2:p.Val742Ala
ENST00000275493.6:c.2225T>C ENSP00000275493.2:p.Val742Ala
ENST00000442591.5:c.*28+1834T>C ENSP00000410031.1:p.=
ENST00000454757.6:c.2090T>C ENSP00000395243.3:p.Val697Ala
ENST00000455089.5:c.2090T>C ENSP00000415559.1:p.Val697Ala
NM_005228.3:c.2225T>C , LRG_304t1:c.2225T>C NP_005219.2:p.Val742Ala
NM_001346897.1:c.2090T>C NP_001333826.1:p.Val697Ala
NM_001346898.1:c.2225T>C NP_001333827.1:p.Val742Ala
NM_001346899.1:c.2090T>C NP_001333828.1:p.Val697Ala
NM_001346900.1:c.2066T>C NP_001333829.1:p.Val689Ala
NM_001346941.1:c.1424T>C NP_001333870.1:p.Val475Ala
NM_005228.4:c.2225T>C NP_005219.2:p.Val742Ala
NM_005228.5:c.2225T>C MANE Select NP_005219.2:p.Val742Ala
NM_001346897.2:c.2090T>C NP_001333826.1:p.Val697Ala
NM_001346898.2:c.2225T>C NP_001333827.1:p.Val742Ala
NM_001346900.2:c.2066T>C NP_001333829.1:p.Val689Ala
NM_001346941.2:c.1424T>C NP_001333870.1:p.Val475Ala
NM_001346899.2:c.2090T>C NP_001333828.1:p.Val697Ala