Linked Data
ClinVar Variation Id:
308054
dbSNP Id:
rs768891600
gnomAD v2:
12-25358231-A-G
gnomAD v3:
12-25205297-A-G
gnomAD v4:
12-25205297-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.25205297A>G , CM000674.2:g.25205297A>G | GRCh38 |
| NC_000012.11:g.25358231A>G , CM000674.1:g.25358231A>G | GRCh37 |
| NC_000012.10:g.25249498A>G | NCBI36 |
| NG_007524.1:g.50624T>C | |
| NG_007524.2:g.50707T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000685328.1:c.*4498T>C (KRAS) | ENSP00000508921.1:n.*4498T>C | |
| ENST00000686877.1:c.*5036T>C (KRAS) | ENSP00000510431.1:n.*5036T>C | |
| ENST00000687356.1:c.*4763T>C (KRAS) | ENSP00000510511.1:n.*4763T>C | |
| ENST00000690406.1:c.4868T>C (KRAS) | ||
| ENST00000693229.1:c.*4498T>C (KRAS) | ENSP00000509223.1:n.*4498T>C | |
| ENST00000256078.10:c.*4619T>C (KRAS) MANE Plus Clinical | ENSP00000256078.5:n.*4619T>C | |
| ENST00000311936.8:c.*4498T>C (KRAS) MANE Select | ENSP00000308495.3:n.*4498T>C | |
| ENST00000553788.6:c.51+1290A>G (ETFRF1) | ENSP00000451938.2:n.51+1290A>G | |
| ENST00000311936.7:c.*4498T>C (KRAS) | ENSP00000308495.3:n.*4498T>C | |
| ENST00000553788.5:c.45+1290A>G (ETFRF1) | ENSP00000451938.1:n.45+1290A>G | |
| NM_004985.4:c.*4498T>C (KRAS) | NP_004976.2:n.*4498T>C | |
| NM_033360.3:c.*4619T>C (KRAS) | NP_203524.1:n.*4619T>C | |
| XM_011520653.1:c.*4498T>C (KRAS) | XP_011518955.1:n.*4498T>C | |
| XM_011520653.3:c.*4498T>C (KRAS) | XP_011518955.1:n.*4498T>C | |
| NM_001369786.1:c.*4619T>C (KRAS) | NP_001356715.1:n.*4619T>C | |
| NM_001369787.1:c.*4498T>C (KRAS) | NP_001356716.1:n.*4498T>C | |
| NM_004985.5:c.*4498T>C (KRAS) MANE Select | NP_004976.2:n.*4498T>C | |
| NM_033360.4:c.*4619T>C (KRAS) MANE Plus Clinical | NP_203524.1:n.*4619T>C |