Linked Data
ClinVar Variation Id:
180848
ClinVar RCV Id:
RCV000157914
RCV000418565
RCV000418712
RCV000427265
RCV000429433
RCV000434580
RCV000436822
RCV000442670
RCV000444507
RCV000419846
RCV000421468
RCV000424767
RCV000426169
RCV000428389
RCV000432148
RCV000437080
RCV000439230
RCV000444587
RCV000590121
RCV001255688
RCV001849323
dbSNP Id:
rs104894226
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.534285C>A , CM000673.2:g.534285C>A | GRCh38 |
| NC_000011.9:g.534285C>A , CM000673.1:g.534285C>A | GRCh37 |
| NC_000011.8:g.524285C>A | NCBI36 |
| NG_007666.1:g.6266G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397594.7:c.38G>T (HRAS) | ENSP00000380722.3:p.Gly13Val | |
| ENST00000417302.7:c.38G>T (HRAS) MANE Plus Clinical | ENSP00000388246.1:p.Gly13Val | |
| ENST00000417302.6:c.38G>T (HRAS) | ENSP00000388246.1:p.Gly13Val | |
| ENST00000462734.2:c.38G>T (HRAS) | ENSP00000507303.1:p.Gly13Val | |
| ENST00000311189.8:c.38G>T (HRAS) MANE Select | ENSP00000309845.7:p.Gly13Val | |
| ENST00000311189.7:c.38G>T (HRAS) | ENSP00000309845.7:p.Gly13Val | |
| ENST00000397594.5:c.38G>T (HRAS) | ENSP00000380722.1:p.Gly13Val | |
| ENST00000397596.6:c.38G>T (HRAS) | ENSP00000380723.2:p.Gly13Val | |
| ENST00000417302.5:c.38G>T (HRAS) | ENSP00000388246.1:p.Gly13Val | |
| ENST00000451590.5:c.38G>T (HRAS) | ENSP00000407586.1:p.Gly13Val | |
| ENST00000468682.2:n.526G>T (HRAS) | ||
| ENST00000482021.1:n.161G>T (HRAS) | ||
| ENST00000493230.5:c.38G>T (HRAS) | ENSP00000434023.1:p.Gly13Val | |
| NM_001130442.1:c.38G>T (HRAS) | NP_001123914.1:p.Gly13Val | |
| NM_005343.2:c.38G>T (HRAS) | NP_005334.1:p.Gly13Val | |
| NM_176795.3:c.38G>T (HRAS) | NP_789765.1:p.Gly13Val | |
| XM_011519875.1:c.-424-4313C>A (LRRC56) | XP_011518177.1:n.-424-4313C>A | |
| XM_011519877.1:c.-161-5295C>A (LRRC56) | XP_011518179.1:n.-161-5295C>A | |
| XR_242795.1:n.237G>T (HRAS) | ||
| NM_001130442.2:c.38G>T (HRAS) | NP_001123914.1:p.Gly13Val | |
| NM_001318054.1:c.-282G>T (HRAS) | NP_001304983.1:n.-282G>T | |
| NM_005343.3:c.38G>T (HRAS) | NP_005334.1:p.Gly13Val | |
| NM_176795.4:c.38G>T (HRAS) | NP_789765.1:p.Gly13Val | |
| XM_011519875.2:c.-424-4313C>A (LRRC56) | XP_011518177.1:n.-424-4313C>A | |
| XM_011519877.2:c.-161-5295C>A (LRRC56) | XP_011518179.1:n.-161-5295C>A | |
| XM_017017167.1:c.-499-4238C>A (LRRC56) | XP_016872656.1:n.-499-4238C>A | |
| XM_017017168.1:c.-499-4238C>A (LRRC56) | XP_016872657.1:n.-499-4238C>A | |
| NM_005343.4:c.38G>T (HRAS) MANE Select | NP_005334.1:p.Gly13Val | |
| NM_001318054.2:c.-282G>T (HRAS) | NP_001304983.1:n.-282G>T | |
| NM_001130442.3:c.38G>T (HRAS) | NP_001123914.1:p.Gly13Val | |
| NM_176795.5:c.38G>T (HRAS) MANE Plus Clinical | NP_789765.1:p.Gly13Val |