gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00039002 (AFR)
Genomes Max Group AF
0.00026359 (EAS)
Exomes Max Group AF
0.0004939 (AFR)
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.533311_533330del , CM000673.2:g.533311_533330del | GRCh38 |
| NC_000011.9:g.533311_533330del , CM000673.1:g.533311_533330del | GRCh37 |
| NC_000011.8:g.523311_523330del | NCBI36 |
| NG_007666.1:g.7230_7249del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397594.7:c.488_507del (HRAS) | ENSP00000380722.3:p.Leu163HisfsTer10 | |
| ENST00000417302.7:c.488_507del (HRAS) MANE Plus Clinical | ENSP00000388246.1:p.Leu163HisfsTer30 | |
| ENST00000397594.6:c.206_225del (HRAS) | ENSP00000380722.2:p.Leu69HisfsTer10 | |
| ENST00000417302.6:c.488_507del (HRAS) | ENSP00000388246.1:p.Leu163HisfsTer30 | |
| ENST00000462734.2:c.*18_*37del (HRAS) | ENSP00000507303.1:n.*18_*37del | |
| ENST00000311189.8:c.450+132_450+151del (HRAS) MANE Select | ENSP00000309845.7:n.450+132_450+151del | |
| ENST00000311189.7:c.450+132_450+151del (HRAS) | ENSP00000309845.7:n.450+132_450+151del | |
| ENST00000397594.5:c.488_507del (HRAS) | ENSP00000380722.1:p.Leu163HisfsTer30 | |
| ENST00000397596.6:c.450+132_450+151del (HRAS) | ENSP00000380723.2:n.450+132_450+151del | |
| ENST00000417302.5:c.488_507del (HRAS) | ENSP00000388246.1:p.Leu163HisfsTer30 | |
| ENST00000451590.5:c.450+132_450+151del (HRAS) | ENSP00000407586.1:n.450+132_450+151del | |
| ENST00000462734.1:n.181_200del (HRAS) | ||
| ENST00000478324.5:n.198_217del (HRAS) | ||
| ENST00000479482.1:n.371+132_371+151del (HRAS) | ||
| ENST00000493230.5:c.488_507del (HRAS) | ENSP00000434023.1:p.Leu163HisfsTer30 | |
| NM_001130442.1:c.450+132_450+151del (HRAS) | NP_001123914.1:n.450+132_450+151del | |
| NM_005343.2:c.450+132_450+151del (HRAS) | NP_005334.1:n.450+132_450+151del | |
| NM_176795.3:c.488_507del (HRAS) | NP_789765.1:p.Leu163HisfsTer30 | |
| XM_011519875.1:c.-425+4974_-425+4993del (LRRC56) | XP_011518177.1:n.-425+4974_-425+4993del | |
| XM_011519877.1:c.-162+4974_-162+4993del (LRRC56) | XP_011518179.1:n.-162+4974_-162+4993del | |
| XR_242795.1:n.687_706del (HRAS) | ||
| NM_001130442.2:c.450+132_450+151del (HRAS) | NP_001123914.1:n.450+132_450+151del | |
| NM_001318054.1:c.169_188del (HRAS) | NP_001304983.1:p.Ser57MetfsTer2 | |
| NM_005343.3:c.450+132_450+151del (HRAS) | NP_005334.1:n.450+132_450+151del | |
| NM_176795.4:c.488_507del (HRAS) | NP_789765.1:p.Leu163HisfsTer30 | |
| XM_011519875.2:c.-425+4974_-425+4993del (LRRC56) | XP_011518177.1:n.-425+4974_-425+4993del | |
| XM_011519877.2:c.-162+4974_-162+4993del (LRRC56) | XP_011518179.1:n.-162+4974_-162+4993del | |
| XM_017017167.1:c.-500+4974_-500+4993del (LRRC56) | XP_016872656.1:n.-500+4974_-500+4993del | |
| XM_017017168.1:c.-500+4974_-500+4993del (LRRC56) | XP_016872657.1:n.-500+4974_-500+4993del | |
| NM_005343.4:c.450+132_450+151del (HRAS) MANE Select | NP_005334.1:n.450+132_450+151del | |
| NM_001318054.2:c.169_188del (HRAS) | NP_001304983.1:p.Ser57MetfsTer2 | |
| NM_001130442.3:c.450+132_450+151del (HRAS) | NP_001123914.1:n.450+132_450+151del | |
| NM_176795.5:c.488_507del (HRAS) MANE Plus Clinical | NP_789765.1:p.Leu163HisfsTer30 |