Linked Data
dbSNP Id:
rs958579383
gnomAD v2:
11-532439-CCTTCCTTG-C
gnomAD v3:
11-532439-CCTTCCTTG-C
gnomAD v4:
11-532439-CCTTCCTTG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.532445_532452del , CM000673.2:g.532445_532452del | GRCh38 |
| NC_000011.9:g.532445_532452del , CM000673.1:g.532445_532452del | GRCh37 |
| NC_000011.8:g.522445_522452del | NCBI36 |
| NG_007666.1:g.8104_8111del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397594.7:c.*203_*210del (HRAS) | ENSP00000380722.3:n.*203_*210del | |
| ENST00000417302.7:c.*328_*335del (HRAS) MANE Plus Clinical | ENSP00000388246.1:n.*328_*335del | |
| ENST00000397594.6:c.434_441del (HRAS) | ENSP00000380722.2:n.434_441del | |
| ENST00000417302.6:c.*328_*335del (HRAS) | ENSP00000388246.1:n.*328_*335del | |
| ENST00000462734.2:c.*263_*270del (HRAS) | ENSP00000507303.1:n.*263_*270del | |
| ENST00000311189.8:c.*81_*88del (HRAS) MANE Select | ENSP00000309845.7:n.*81_*88del | |
| ENST00000311189.7:c.*81_*88del (HRAS) | ENSP00000309845.7:n.*81_*88del | |
| ENST00000397594.5:c.*328_*335del (HRAS) | ENSP00000380722.1:n.*328_*335del | |
| ENST00000397596.6:c.*189_*196del (HRAS) | ENSP00000380723.2:n.*189_*196del | |
| ENST00000417302.5:c.*328_*335del (HRAS) | ENSP00000388246.1:n.*328_*335del | |
| ENST00000451590.5:c.*189_*196del (HRAS) | ENSP00000407586.1:n.*189_*196del | |
| ENST00000462734.1:n.426_433del (HRAS) | ||
| ENST00000478324.5:n.426_433del (HRAS) | ||
| ENST00000493230.5:c.*220_*227del (HRAS) | ENSP00000434023.1:n.*220_*227del | |
| NM_001130442.1:c.*189_*196del (HRAS) | NP_001123914.1:n.*189_*196del | |
| NM_005343.2:c.*81_*88del (HRAS) | NP_005334.1:n.*81_*88del | |
| NM_176795.3:c.*328_*335del (HRAS) | NP_789765.1:n.*328_*335del | |
| XM_011519875.1:c.-425+4108_-425+4115del (LRRC56) | XP_011518177.1:n.-425+4108_-425+4115del | |
| XM_011519877.1:c.-162+4108_-162+4115del (LRRC56) | XP_011518179.1:n.-162+4108_-162+4115del | |
| XR_242795.1:n.932_939del (HRAS) | ||
| NM_001130442.2:c.*189_*196del (HRAS) | NP_001123914.1:n.*189_*196del | |
| NM_001318054.1:c.*81_*88del (HRAS) | NP_001304983.1:n.*81_*88del | |
| NM_005343.3:c.*81_*88del (HRAS) | NP_005334.1:n.*81_*88del | |
| NM_176795.4:c.*328_*335del (HRAS) | NP_789765.1:n.*328_*335del | |
| XM_011519875.2:c.-425+4108_-425+4115del (LRRC56) | XP_011518177.1:n.-425+4108_-425+4115del | |
| XM_011519877.2:c.-162+4108_-162+4115del (LRRC56) | XP_011518179.1:n.-162+4108_-162+4115del | |
| XM_017017167.1:c.-500+4108_-500+4115del (LRRC56) | XP_016872656.1:n.-500+4108_-500+4115del | |
| XM_017017168.1:c.-500+4108_-500+4115del (LRRC56) | XP_016872657.1:n.-500+4108_-500+4115del | |
| NM_005343.4:c.*81_*88del (HRAS) MANE Select | NP_005334.1:n.*81_*88del | |
| NM_001318054.2:c.*81_*88del (HRAS) | NP_001304983.1:n.*81_*88del | |
| NM_001130442.3:c.*189_*196del (HRAS) | NP_001123914.1:n.*189_*196del | |
| NM_176795.5:c.*328_*335del (HRAS) MANE Plus Clinical | NP_789765.1:n.*328_*335del |