Linked Data
ClinVar Variation Id:
308083
dbSNP Id:
rs886049185
gnomAD v2:
12-25360035-G-A
gnomAD v3:
12-25207101-G-A
gnomAD v4:
12-25207101-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.25207101G>A , CM000674.2:g.25207101G>A | GRCh38 |
| NC_000012.11:g.25360035G>A , CM000674.1:g.25360035G>A | GRCh37 |
| NC_000012.10:g.25251302G>A | NCBI36 |
| NG_007524.1:g.48820C>T | |
| NG_007524.2:g.48903C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000685328.1:c.*2694C>T (KRAS) | ENSP00000508921.1:n.*2694C>T | |
| ENST00000686877.1:c.*3232C>T (KRAS) | ENSP00000510431.1:n.*3232C>T | |
| ENST00000687356.1:c.*2959C>T (KRAS) | ENSP00000510511.1:n.*2959C>T | |
| ENST00000688940.1:c.*2694C>T (KRAS) | ENSP00000509238.1:n.*2694C>T | |
| ENST00000690406.1:c.3064C>T (KRAS) | ||
| ENST00000692768.1:c.*2694C>T (KRAS) | ENSP00000510254.1:n.*2694C>T | |
| ENST00000693229.1:c.*2694C>T (KRAS) | ENSP00000509223.1:n.*2694C>T | |
| ENST00000256078.10:c.*2815C>T (KRAS) MANE Plus Clinical | ENSP00000256078.5:n.*2815C>T | |
| ENST00000311936.8:c.*2694C>T (KRAS) MANE Select | ENSP00000308495.3:n.*2694C>T | |
| ENST00000553788.6:c.52-2094G>A (ETFRF1) | ENSP00000451938.2:n.52-2094G>A | |
| ENST00000311936.7:c.*2694C>T (KRAS) | ENSP00000308495.3:n.*2694C>T | |
| ENST00000553788.5:c.46-2094G>A (ETFRF1) | ENSP00000451938.1:n.46-2094G>A | |
| NM_004985.4:c.*2694C>T (KRAS) | NP_004976.2:n.*2694C>T | |
| NM_033360.3:c.*2815C>T (KRAS) | NP_203524.1:n.*2815C>T | |
| XM_011520653.1:c.*2694C>T (KRAS) | XP_011518955.1:n.*2694C>T | |
| XM_011520653.3:c.*2694C>T (KRAS) | XP_011518955.1:n.*2694C>T | |
| NM_001369786.1:c.*2815C>T (KRAS) | NP_001356715.1:n.*2815C>T | |
| NM_001369787.1:c.*2694C>T (KRAS) | NP_001356716.1:n.*2694C>T | |
| NM_004985.5:c.*2694C>T (KRAS) MANE Select | NP_004976.2:n.*2694C>T | |
| NM_033360.4:c.*2815C>T (KRAS) MANE Plus Clinical | NP_203524.1:n.*2815C>T |