Linked Data
ClinVar Variation Id:
376083
ClinVar RCV Id:
RCV000420488
dbSNP Id:
rs121913432
COSMIC:
COSM13433
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.55181327A>G , CM000669.2:g.55181327A>G | GRCh38 |
| NC_000007.13:g.55249020A>G , CM000669.1:g.55249020A>G | GRCh37 |
| NC_000007.12:g.55216514A>G | NCBI36 |
| NG_007726.3:g.167296A>G , LRG_304:g.167296A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000450046.2:c.2159A>G (EGFR) | ENSP00000413354.2:p.His720Arg | |
| ENST00000700145.1:c.667A>G (EGFR) | ||
| ENST00000275493.7:c.2318A>G (EGFR) MANE Select | ENSP00000275493.2:p.His773Arg | |
| ENST00000275493.6:c.2318A>G (EGFR) | ENSP00000275493.2:p.His773Arg | |
| ENST00000442591.5:c.*28+8399A>G (EGFR) | ENSP00000410031.1:n.*28+8399A>G | |
| ENST00000454757.6:c.2183A>G (EGFR) | ENSP00000395243.3:p.His728Arg | |
| ENST00000455089.5:c.2183A>G (EGFR) | ENSP00000415559.1:p.His728Arg | |
| NM_005228.3:c.2318A>G , LRG_304t1:c.2318A>G (EGFR) | NP_005219.2:p.His773Arg | |
| NR_047551.1:n.1244T>C (EGFR-AS1) | ||
| NM_001346897.1:c.2183A>G (EGFR) | NP_001333826.1:p.His728Arg | |
| NM_001346898.1:c.2318A>G (EGFR) | NP_001333827.1:p.His773Arg | |
| NM_001346899.1:c.2183A>G (EGFR) | NP_001333828.1:p.His728Arg | |
| NM_001346900.1:c.2159A>G (EGFR) | NP_001333829.1:p.His720Arg | |
| NM_001346941.1:c.1517A>G (EGFR) | NP_001333870.1:p.His506Arg | |
| NM_005228.4:c.2318A>G (EGFR) | NP_005219.2:p.His773Arg | |
| NM_005228.5:c.2318A>G (EGFR) MANE Select | NP_005219.2:p.His773Arg | |
| NM_001346897.2:c.2183A>G (EGFR) | NP_001333826.1:p.His728Arg | |
| NM_001346898.2:c.2318A>G (EGFR) | NP_001333827.1:p.His773Arg | |
| NM_001346900.2:c.2159A>G (EGFR) | NP_001333829.1:p.His720Arg | |
| NM_001346941.2:c.1517A>G (EGFR) | NP_001333870.1:p.His506Arg | |
| NM_001346899.2:c.2183A>G (EGFR) | NP_001333828.1:p.His728Arg |