Linked Data
ClinVar Variation Id:
308072
ClinVar RCV Id:
RCV000318890
dbSNP Id:
rs61764372
gnomAD v2:
12-25359227-A-T
gnomAD v3:
12-25206293-A-T
gnomAD v4:
12-25206293-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.25206293A>T , CM000674.2:g.25206293A>T | GRCh38 |
| NC_000012.11:g.25359227A>T , CM000674.1:g.25359227A>T | GRCh37 |
| NC_000012.10:g.25250494A>T | NCBI36 |
| NG_007524.1:g.49628T>A | |
| NG_007524.2:g.49711T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000685328.1:c.*3502T>A (KRAS) | ENSP00000508921.1:n.*3502T>A | |
| ENST00000686877.1:c.*4040T>A (KRAS) | ENSP00000510431.1:n.*4040T>A | |
| ENST00000687356.1:c.*3767T>A (KRAS) | ENSP00000510511.1:n.*3767T>A | |
| ENST00000690406.1:c.3872T>A (KRAS) | ||
| ENST00000692768.1:c.*3502T>A (KRAS) | ENSP00000510254.1:n.*3502T>A | |
| ENST00000693229.1:c.*3502T>A (KRAS) | ENSP00000509223.1:n.*3502T>A | |
| ENST00000256078.10:c.*3623T>A (KRAS) MANE Plus Clinical | ENSP00000256078.5:n.*3623T>A | |
| ENST00000311936.8:c.*3502T>A (KRAS) MANE Select | ENSP00000308495.3:n.*3502T>A | |
| ENST00000553788.6:c.51+2286A>T (ETFRF1) | ENSP00000451938.2:n.51+2286A>T | |
| ENST00000311936.7:c.*3502T>A (KRAS) | ENSP00000308495.3:n.*3502T>A | |
| ENST00000553788.5:c.45+2286A>T (ETFRF1) | ENSP00000451938.1:n.45+2286A>T | |
| NM_004985.4:c.*3502T>A (KRAS) | NP_004976.2:n.*3502T>A | |
| NM_033360.3:c.*3623T>A (KRAS) | NP_203524.1:n.*3623T>A | |
| XM_011520653.1:c.*3502T>A (KRAS) | XP_011518955.1:n.*3502T>A | |
| XM_011520653.3:c.*3502T>A (KRAS) | XP_011518955.1:n.*3502T>A | |
| NM_001369786.1:c.*3623T>A (KRAS) | NP_001356715.1:n.*3623T>A | |
| NM_001369787.1:c.*3502T>A (KRAS) | NP_001356716.1:n.*3502T>A | |
| NM_004985.5:c.*3502T>A (KRAS) MANE Select | NP_004976.2:n.*3502T>A | |
| NM_033360.4:c.*3623T>A (KRAS) MANE Plus Clinical | NP_203524.1:n.*3623T>A |