Linked Data
ClinVar Variation Id:
40437
ClinVar RCV Id:
RCV000154506
RCV000519779
RCV000680288
RCV001085194
RCV001261051
RCV001813234
RCV002257370
RCV003944864
dbSNP Id:
rs138272051
ExAC:
11:533799 T / G
gnomAD v2:
11-533799-T-G
gnomAD v3:
11-533799-T-G
gnomAD v4:
11-533799-T-G
ERepo:
CA180888/MONDO:0021060/004
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.533799T>G , CM000673.2:g.533799T>G | GRCh38 |
| NC_000011.9:g.533799T>G , CM000673.1:g.533799T>G | GRCh37 |
| NC_000011.8:g.523799T>G | NCBI36 |
| NG_007666.1:g.6752A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397594.7:c.257A>C (HRAS) | ENSP00000380722.3:p.Asn86Thr | |
| ENST00000417302.7:c.257A>C (HRAS) MANE Plus Clinical | ENSP00000388246.1:p.Asn86Thr | |
| ENST00000417302.6:c.257A>C (HRAS) | ENSP00000388246.1:p.Asn86Thr | |
| ENST00000462734.2:c.257A>C (HRAS) | ENSP00000507303.1:p.Asn86Thr | |
| ENST00000311189.8:c.257A>C (HRAS) MANE Select | ENSP00000309845.7:p.Asn86Thr | |
| ENST00000311189.7:c.257A>C (HRAS) | ENSP00000309845.7:p.Asn86Thr | |
| ENST00000397594.5:c.257A>C (HRAS) | ENSP00000380722.1:p.Asn86Thr | |
| ENST00000397596.6:c.257A>C (HRAS) | ENSP00000380723.2:p.Asn86Thr | |
| ENST00000417302.5:c.257A>C (HRAS) | ENSP00000388246.1:p.Asn86Thr | |
| ENST00000451590.5:c.257A>C (HRAS) | ENSP00000407586.1:p.Asn86Thr | |
| ENST00000468682.2:n.745A>C (HRAS) | ||
| ENST00000479482.1:n.178A>C (HRAS) | ||
| ENST00000493230.5:c.257A>C (HRAS) | ENSP00000434023.1:p.Asn86Thr | |
| NM_001130442.1:c.257A>C (HRAS) | NP_001123914.1:p.Asn86Thr | |
| NM_005343.2:c.257A>C (HRAS) | NP_005334.1:p.Asn86Thr | |
| NM_176795.3:c.257A>C (HRAS) | NP_789765.1:p.Asn86Thr | |
| XM_011519875.1:c.-424-4799T>G (LRRC56) | XP_011518177.1:n.-424-4799T>G | |
| XM_011519877.1:c.-162+5462T>G (LRRC56) | XP_011518179.1:n.-162+5462T>G | |
| XR_242795.1:n.456A>C (HRAS) | ||
| NM_001130442.2:c.257A>C (HRAS) | NP_001123914.1:p.Asn86Thr | |
| NM_001318054.1:c.-63A>C (HRAS) | NP_001304983.1:n.-63A>C | |
| NM_005343.3:c.257A>C (HRAS) | NP_005334.1:p.Asn86Thr | |
| NM_176795.4:c.257A>C (HRAS) | NP_789765.1:p.Asn86Thr | |
| XM_011519875.2:c.-424-4799T>G (LRRC56) | XP_011518177.1:n.-424-4799T>G | |
| XM_011519877.2:c.-162+5462T>G (LRRC56) | XP_011518179.1:n.-162+5462T>G | |
| XM_017017167.1:c.-499-4724T>G (LRRC56) | XP_016872656.1:n.-499-4724T>G | |
| XM_017017168.1:c.-499-4724T>G (LRRC56) | XP_016872657.1:n.-499-4724T>G | |
| NM_005343.4:c.257A>C (HRAS) MANE Select | NP_005334.1:p.Asn86Thr | |
| NM_001318054.2:c.-63A>C (HRAS) | NP_001304983.1:n.-63A>C | |
| NM_001130442.3:c.257A>C (HRAS) | NP_001123914.1:p.Asn86Thr | |
| NM_176795.5:c.257A>C (HRAS) MANE Plus Clinical | NP_789765.1:p.Asn86Thr |