Linked Data
ClinVar Variation Id:
308073
ClinVar RCV Id:
RCV000278974
dbSNP Id:
rs886049181
gnomAD v2:
12-25359230-G-A
gnomAD v3:
12-25206296-G-A
gnomAD v4:
12-25206296-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.25206296G>A , CM000674.2:g.25206296G>A | GRCh38 |
| NC_000012.11:g.25359230G>A , CM000674.1:g.25359230G>A | GRCh37 |
| NC_000012.10:g.25250497G>A | NCBI36 |
| NG_007524.1:g.49625C>T | |
| NG_007524.2:g.49708C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000685328.1:c.*3499C>T (KRAS) | ENSP00000508921.1:n.*3499C>T | |
| ENST00000686877.1:c.*4037C>T (KRAS) | ENSP00000510431.1:n.*4037C>T | |
| ENST00000687356.1:c.*3764C>T (KRAS) | ENSP00000510511.1:n.*3764C>T | |
| ENST00000690406.1:c.3869C>T (KRAS) | ||
| ENST00000692768.1:c.*3499C>T (KRAS) | ENSP00000510254.1:n.*3499C>T | |
| ENST00000693229.1:c.*3499C>T (KRAS) | ENSP00000509223.1:n.*3499C>T | |
| ENST00000256078.10:c.*3620C>T (KRAS) MANE Plus Clinical | ENSP00000256078.5:n.*3620C>T | |
| ENST00000311936.8:c.*3499C>T (KRAS) MANE Select | ENSP00000308495.3:n.*3499C>T | |
| ENST00000553788.6:c.51+2289G>A (ETFRF1) | ENSP00000451938.2:n.51+2289G>A | |
| ENST00000311936.7:c.*3499C>T (KRAS) | ENSP00000308495.3:n.*3499C>T | |
| ENST00000553788.5:c.45+2289G>A (ETFRF1) | ENSP00000451938.1:n.45+2289G>A | |
| NM_004985.4:c.*3499C>T (KRAS) | NP_004976.2:n.*3499C>T | |
| NM_033360.3:c.*3620C>T (KRAS) | NP_203524.1:n.*3620C>T | |
| XM_011520653.1:c.*3499C>T (KRAS) | XP_011518955.1:n.*3499C>T | |
| XM_011520653.3:c.*3499C>T (KRAS) | XP_011518955.1:n.*3499C>T | |
| NM_001369786.1:c.*3620C>T (KRAS) | NP_001356715.1:n.*3620C>T | |
| NM_001369787.1:c.*3499C>T (KRAS) | NP_001356716.1:n.*3499C>T | |
| NM_004985.5:c.*3499C>T (KRAS) MANE Select | NP_004976.2:n.*3499C>T | |
| NM_033360.4:c.*3620C>T (KRAS) MANE Plus Clinical | NP_203524.1:n.*3620C>T |