Linked Data
dbSNP Id:
rs771756228
gnomAD v2:
11-533976-AGGACCTTCCGTGG-A
gnomAD v4:
11-533976-AGGACCTTCCGTGG-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.533979_533991del , CM000673.2:g.533979_533991del | GRCh38 |
| NC_000011.9:g.533979_533991del , CM000673.1:g.533979_533991del | GRCh37 |
| NC_000011.8:g.523979_523991del | NCBI36 |
| NG_007666.1:g.6562_6574del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397594.7:c.112-45_112-33del (HRAS) | ENSP00000380722.3:n.112-45_112-33del | |
| ENST00000417302.7:c.112-45_112-33del (HRAS) MANE Plus Clinical | ENSP00000388246.1:n.112-45_112-33del | |
| ENST00000417302.6:c.112-45_112-33del (HRAS) | ENSP00000388246.1:n.112-45_112-33del | |
| ENST00000462734.2:c.112-45_112-33del (HRAS) | ENSP00000507303.1:n.112-45_112-33del | |
| ENST00000311189.8:c.112-45_112-33del (HRAS) MANE Select | ENSP00000309845.7:n.112-45_112-33del | |
| ENST00000311189.7:c.112-45_112-33del (HRAS) | ENSP00000309845.7:n.112-45_112-33del | |
| ENST00000397594.5:c.112-45_112-33del (HRAS) | ENSP00000380722.1:n.112-45_112-33del | |
| ENST00000397596.6:c.112-45_112-33del (HRAS) | ENSP00000380723.2:n.112-45_112-33del | |
| ENST00000417302.5:c.112-45_112-33del (HRAS) | ENSP00000388246.1:n.112-45_112-33del | |
| ENST00000451590.5:c.112-45_112-33del (HRAS) | ENSP00000407586.1:n.112-45_112-33del | |
| ENST00000468682.2:n.600-45_600-33del (HRAS) | ||
| ENST00000493230.5:c.112-45_112-33del (HRAS) | ENSP00000434023.1:n.112-45_112-33del | |
| NM_001130442.1:c.112-45_112-33del (HRAS) | NP_001123914.1:n.112-45_112-33del | |
| NM_005343.2:c.112-45_112-33del (HRAS) | NP_005334.1:n.112-45_112-33del | |
| NM_176795.3:c.112-45_112-33del (HRAS) | NP_789765.1:n.112-45_112-33del | |
| XM_011519875.1:c.-424-4619_-424-4607del (LRRC56) | XP_011518177.1:n.-424-4619_-424-4607del | |
| XM_011519877.1:c.-161-5601_-161-5589del (LRRC56) | XP_011518179.1:n.-161-5601_-161-5589del | |
| XR_242795.1:n.311-45_311-33del (HRAS) | ||
| NM_001130442.2:c.112-45_112-33del (HRAS) | NP_001123914.1:n.112-45_112-33del | |
| NM_001318054.1:c.-208-45_-208-33del (HRAS) | NP_001304983.1:n.-208-45_-208-33del | |
| NM_005343.3:c.112-45_112-33del (HRAS) | NP_005334.1:n.112-45_112-33del | |
| NM_176795.4:c.112-45_112-33del (HRAS) | NP_789765.1:n.112-45_112-33del | |
| XM_011519875.2:c.-424-4619_-424-4607del (LRRC56) | XP_011518177.1:n.-424-4619_-424-4607del | |
| XM_011519877.2:c.-161-5601_-161-5589del (LRRC56) | XP_011518179.1:n.-161-5601_-161-5589del | |
| XM_017017167.1:c.-499-4544_-499-4532del (LRRC56) | XP_016872656.1:n.-499-4544_-499-4532del | |
| XM_017017168.1:c.-499-4544_-499-4532del (LRRC56) | XP_016872657.1:n.-499-4544_-499-4532del | |
| NM_005343.4:c.112-45_112-33del (HRAS) MANE Select | NP_005334.1:n.112-45_112-33del | |
| NM_001318054.2:c.-208-45_-208-33del (HRAS) | NP_001304983.1:n.-208-45_-208-33del | |
| NM_001130442.3:c.112-45_112-33del (HRAS) | NP_001123914.1:n.112-45_112-33del | |
| NM_176795.5:c.112-45_112-33del (HRAS) MANE Plus Clinical | NP_789765.1:n.112-45_112-33del |