Linked Data
ClinVar Variation Id:
308093
ClinVar RCV Id:
RCV000323774
dbSNP Id:
rs886049190
gnomAD v2:
12-25360838-A-G
gnomAD v3:
12-25207904-A-G
gnomAD v4:
12-25207904-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.25207904A>G , CM000674.2:g.25207904A>G | GRCh38 |
| NC_000012.11:g.25360838A>G , CM000674.1:g.25360838A>G | GRCh37 |
| NC_000012.10:g.25252105A>G | NCBI36 |
| NG_007524.1:g.48017T>C | |
| NG_007524.2:g.48100T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000685328.1:c.*1891T>C (KRAS) | ENSP00000508921.1:n.*1891T>C | |
| ENST00000686877.1:c.*2429T>C (KRAS) | ENSP00000510431.1:n.*2429T>C | |
| ENST00000687356.1:c.*2156T>C (KRAS) | ENSP00000510511.1:n.*2156T>C | |
| ENST00000688940.1:c.*1891T>C (KRAS) | ENSP00000509238.1:n.*1891T>C | |
| ENST00000690406.1:c.2261T>C (KRAS) | ||
| ENST00000692768.1:c.*1891T>C (KRAS) | ENSP00000510254.1:n.*1891T>C | |
| ENST00000693229.1:c.*1891T>C (KRAS) | ENSP00000509223.1:n.*1891T>C | |
| ENST00000256078.10:c.*2012T>C (KRAS) MANE Plus Clinical | ENSP00000256078.5:n.*2012T>C | |
| ENST00000311936.8:c.*1891T>C (KRAS) MANE Select | ENSP00000308495.3:n.*1891T>C | |
| ENST00000553788.6:c.52-1291A>G (ETFRF1) | ENSP00000451938.2:n.52-1291A>G | |
| ENST00000311936.7:c.*1891T>C (KRAS) | ENSP00000308495.3:n.*1891T>C | |
| ENST00000553788.5:c.46-1291A>G (ETFRF1) | ENSP00000451938.1:n.46-1291A>G | |
| NM_004985.4:c.*1891T>C (KRAS) | NP_004976.2:n.*1891T>C | |
| NM_033360.3:c.*2012T>C (KRAS) | NP_203524.1:n.*2012T>C | |
| XM_011520653.1:c.*1891T>C (KRAS) | XP_011518955.1:n.*1891T>C | |
| XM_011520653.3:c.*1891T>C (KRAS) | XP_011518955.1:n.*1891T>C | |
| NM_001369786.1:c.*2012T>C (KRAS) | NP_001356715.1:n.*2012T>C | |
| NM_001369787.1:c.*1891T>C (KRAS) | NP_001356716.1:n.*1891T>C | |
| NM_004985.5:c.*1891T>C (KRAS) MANE Select | NP_004976.2:n.*1891T>C | |
| NM_033360.4:c.*2012T>C (KRAS) MANE Plus Clinical | NP_203524.1:n.*2012T>C |