Linked Data
ClinVar Variation Id:
134514
dbSNP Id:
rs587778400
gnomAD v2:
11-532733-G-A
gnomAD v4:
11-532733-G-A
PubMed:
PMID:24728327
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.532733G>A , CM000673.2:g.532733G>A | GRCh38 |
| NC_000011.9:g.532733G>A , CM000673.1:g.532733G>A | GRCh37 |
| NC_000011.8:g.522733G>A | NCBI36 |
| NG_007666.1:g.7818C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397594.7:c.*20-103C>T (HRAS) | ENSP00000380722.3:n.*20-103C>T | |
| ENST00000417302.7:c.*42C>T (HRAS) MANE Plus Clinical | ENSP00000388246.1:n.*42C>T | |
| ENST00000397594.6:c.251-103C>T (HRAS) | ENSP00000380722.2:n.251-103C>T | |
| ENST00000417302.6:c.*42C>T (HRAS) | ENSP00000388246.1:n.*42C>T | |
| ENST00000462734.2:c.*85C>T (HRAS) | ENSP00000507303.1:n.*85C>T | |
| ENST00000311189.8:c.473C>T (HRAS) MANE Select | ENSP00000309845.7:p.Thr158Met | |
| ENST00000311189.7:c.473C>T (HRAS) | ENSP00000309845.7:p.Thr158Met | |
| ENST00000397594.5:c.*42C>T (HRAS) | ENSP00000380722.1:n.*42C>T | |
| ENST00000397596.6:c.473C>T (HRAS) | ENSP00000380723.2:p.Thr158Met | |
| ENST00000417302.5:c.*42C>T (HRAS) | ENSP00000388246.1:n.*42C>T | |
| ENST00000451590.5:c.473C>T (HRAS) | ENSP00000407586.1:p.Thr158Met | |
| ENST00000462734.1:n.248C>T (HRAS) | ||
| ENST00000478324.5:n.243-103C>T (HRAS) | ||
| ENST00000479482.1:n.394C>T (HRAS) | ||
| ENST00000493230.5:c.*42C>T (HRAS) | ENSP00000434023.1:n.*42C>T | |
| NM_001130442.1:c.473C>T (HRAS) | NP_001123914.1:p.Thr158Met | |
| NM_005343.2:c.473C>T (HRAS) | NP_005334.1:p.Thr158Met | |
| NM_176795.3:c.*42C>T (HRAS) | NP_789765.1:n.*42C>T | |
| XM_011519875.1:c.-425+4396G>A (LRRC56) | XP_011518177.1:n.-425+4396G>A | |
| XM_011519877.1:c.-162+4396G>A (LRRC56) | XP_011518179.1:n.-162+4396G>A | |
| XR_242795.1:n.754C>T (HRAS) | ||
| NM_001130442.2:c.473C>T (HRAS) | NP_001123914.1:p.Thr158Met | |
| NM_001318054.1:c.236C>T (HRAS) | NP_001304983.1:p.Thr79Met | |
| NM_005343.3:c.473C>T (HRAS) | NP_005334.1:p.Thr158Met | |
| NM_176795.4:c.*42C>T (HRAS) | NP_789765.1:n.*42C>T | |
| XM_011519875.2:c.-425+4396G>A (LRRC56) | XP_011518177.1:n.-425+4396G>A | |
| XM_011519877.2:c.-162+4396G>A (LRRC56) | XP_011518179.1:n.-162+4396G>A | |
| XM_017017167.1:c.-500+4396G>A (LRRC56) | XP_016872656.1:n.-500+4396G>A | |
| XM_017017168.1:c.-500+4396G>A (LRRC56) | XP_016872657.1:n.-500+4396G>A | |
| NM_005343.4:c.473C>T (HRAS) MANE Select | NP_005334.1:p.Thr158Met | |
| NM_001318054.2:c.236C>T (HRAS) | NP_001304983.1:p.Thr79Met | |
| NM_001130442.3:c.473C>T (HRAS) | NP_001123914.1:p.Thr158Met | |
| NM_176795.5:c.*42C>T (HRAS) MANE Plus Clinical | NP_789765.1:n.*42C>T |