Linked Data
ClinVar Variation Id:
35554
ClinVar RCV Id:
RCV000029213
RCV000029212
RCV000032852
RCV000173006
RCV000173005
RCV000422625
RCV000427669
RCV000430227
RCV000437649
RCV000443949
RCV000418725
RCV000420422
RCV000420481
RCV000432361
RCV000439826
RCV000424371
RCV000431824
RCV000419344
RCV000430065
RCV000435072
RCV000439525
RCV000440902
RCV001781319
RCV001813211
RCV001255682
RCV001376004
RCV001849283
RCV003458340
dbSNP Id:
rs104894228
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.534286C>G , CM000673.2:g.534286C>G | GRCh38 |
| NC_000011.9:g.534286C>G , CM000673.1:g.534286C>G | GRCh37 |
| NC_000011.8:g.524286C>G | NCBI36 |
| NG_007666.1:g.6265G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397594.7:c.37G>C (HRAS) | ENSP00000380722.3:p.Gly13Arg | |
| ENST00000417302.7:c.37G>C (HRAS) MANE Plus Clinical | ENSP00000388246.1:p.Gly13Arg | |
| ENST00000417302.6:c.37G>C (HRAS) | ENSP00000388246.1:p.Gly13Arg | |
| ENST00000462734.2:c.37G>C (HRAS) | ENSP00000507303.1:p.Gly13Arg | |
| ENST00000311189.8:c.37G>C (HRAS) MANE Select | ENSP00000309845.7:p.Gly13Arg | |
| ENST00000311189.7:c.37G>C (HRAS) | ENSP00000309845.7:p.Gly13Arg | |
| ENST00000397594.5:c.37G>C (HRAS) | ENSP00000380722.1:p.Gly13Arg | |
| ENST00000397596.6:c.37G>C (HRAS) | ENSP00000380723.2:p.Gly13Arg | |
| ENST00000417302.5:c.37G>C (HRAS) | ENSP00000388246.1:p.Gly13Arg | |
| ENST00000451590.5:c.37G>C (HRAS) | ENSP00000407586.1:p.Gly13Arg | |
| ENST00000468682.2:n.525G>C (HRAS) | ||
| ENST00000482021.1:n.160G>C (HRAS) | ||
| ENST00000493230.5:c.37G>C (HRAS) | ENSP00000434023.1:p.Gly13Arg | |
| NM_001130442.1:c.37G>C (HRAS) | NP_001123914.1:p.Gly13Arg | |
| NM_005343.2:c.37G>C (HRAS) | NP_005334.1:p.Gly13Arg | |
| NM_176795.3:c.37G>C (HRAS) | NP_789765.1:p.Gly13Arg | |
| XM_011519875.1:c.-424-4312C>G (LRRC56) | XP_011518177.1:n.-424-4312C>G | |
| XM_011519877.1:c.-161-5294C>G (LRRC56) | XP_011518179.1:n.-161-5294C>G | |
| XR_242795.1:n.236G>C (HRAS) | ||
| NM_001130442.2:c.37G>C (HRAS) | NP_001123914.1:p.Gly13Arg | |
| NM_001318054.1:c.-283G>C (HRAS) | NP_001304983.1:n.-283G>C | |
| NM_005343.3:c.37G>C (HRAS) | NP_005334.1:p.Gly13Arg | |
| NM_176795.4:c.37G>C (HRAS) | NP_789765.1:p.Gly13Arg | |
| XM_011519875.2:c.-424-4312C>G (LRRC56) | XP_011518177.1:n.-424-4312C>G | |
| XM_011519877.2:c.-161-5294C>G (LRRC56) | XP_011518179.1:n.-161-5294C>G | |
| XM_017017167.1:c.-499-4237C>G (LRRC56) | XP_016872656.1:n.-499-4237C>G | |
| XM_017017168.1:c.-499-4237C>G (LRRC56) | XP_016872657.1:n.-499-4237C>G | |
| NM_005343.4:c.37G>C (HRAS) MANE Select | NP_005334.1:p.Gly13Arg | |
| NM_001318054.2:c.-283G>C (HRAS) | NP_001304983.1:n.-283G>C | |
| NM_001130442.3:c.37G>C (HRAS) | NP_001123914.1:p.Gly13Arg | |
| NM_176795.5:c.37G>C (HRAS) MANE Plus Clinical | NP_789765.1:p.Gly13Arg |