Canonical Allele Identifier: CA1947140744

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532540_532554delinsGAGGCTGCTGACCGC , CM000673.2:g.532540_532554delinsGAGGCTGCTGACCGC GRCh38
NC_000011.9:g.532540_532554delinsGAGGCTGCTGACCGC , CM000673.1:g.532540_532554delinsGAGGCTGCTGACCGC GRCh37
NC_000011.8:g.522540_522554delinsGAGGCTGCTGACCGC NCBI36
NG_007666.1:g.7997_8011delinsGCGGTCAGCAGCCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*96_*110delinsGCGGTCAGCAGCCTC (HRAS) ENSP00000380722.3:n.*96_*110delinsGCGGTCAGCAGCCTC
ENST00000417302.7:c.*221_*235delinsGCGGTCAGCAGCCTC (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*221_*235delinsGCGGTCAGCAGCCTC
ENST00000397594.6:c.327_341delinsGCGGTCAGCAGCCTC (HRAS) ENSP00000380722.2:n.327_341delinsGCGGTCAGCAGCCTC
ENST00000417302.6:c.*221_*235delinsGCGGTCAGCAGCCTC (HRAS) ENSP00000388246.1:n.*221_*235delinsGCGGTCAGCAGCCTC
ENST00000462734.2:c.*188-32_*188-18delinsGCGGTCAGCAGCCTC (HRAS) ENSP00000507303.1:n.*188-32_*188-18delinsGCGGTCAGCAGCCTC
ENST00000311189.8:c.*6-32_*6-18delinsGCGGTCAGCAGCCTC (HRAS) MANE Select ENSP00000309845.7:n.*6-32_*6-18delinsGCGGTCAGCAGCCTC
ENST00000311189.7:c.*6-32_*6-18delinsGCGGTCAGCAGCCTC (HRAS) ENSP00000309845.7:n.*6-32_*6-18delinsGCGGTCAGCAGCCTC
ENST00000397594.5:c.*221_*235delinsGCGGTCAGCAGCCTC (HRAS) ENSP00000380722.1:n.*221_*235delinsGCGGTCAGCAGCCTC
ENST00000397596.6:c.*82_*96delinsGCGGTCAGCAGCCTC (HRAS) ENSP00000380723.2:n.*82_*96delinsGCGGTCAGCAGCCTC
ENST00000417302.5:c.*221_*235delinsGCGGTCAGCAGCCTC (HRAS) ENSP00000388246.1:n.*221_*235delinsGCGGTCAGCAGCCTC
ENST00000451590.5:c.*82_*96delinsGCGGTCAGCAGCCTC (HRAS) ENSP00000407586.1:n.*82_*96delinsGCGGTCAGCAGCCTC
ENST00000462734.1:n.351-32_351-18delinsGCGGTCAGCAGCCTC (HRAS)
ENST00000478324.5:n.319_333delinsGCGGTCAGCAGCCTC (HRAS)
ENST00000493230.5:c.*145-32_*145-18delinsGCGGTCAGCAGCCTC (HRAS) ENSP00000434023.1:n.*145-32_*145-18delinsGCGGTCAGCAGCCTC
NM_001130442.1:c.*82_*96delinsGCGGTCAGCAGCCTC (HRAS) NP_001123914.1:n.*82_*96delinsGCGGTCAGCAGCCTC
NM_005343.2:c.*6-32_*6-18delinsGCGGTCAGCAGCCTC (HRAS) NP_005334.1:n.*6-32_*6-18delinsGCGGTCAGCAGCCTC
NM_176795.3:c.*221_*235delinsGCGGTCAGCAGCCTC (HRAS) NP_789765.1:n.*221_*235delinsGCGGTCAGCAGCCTC
XM_011519875.1:c.-425+4203_-425+4217delinsGAGGCTGCTGACCGC (LRRC56) XP_011518177.1:n.-425+4203_-425+4217delinsGAGGCTGCTGACCGC
XM_011519877.1:c.-162+4203_-162+4217delinsGAGGCTGCTGACCGC (LRRC56) XP_011518179.1:n.-162+4203_-162+4217delinsGAGGCTGCTGACCGC
XR_242795.1:n.857-32_857-18delinsGCGGTCAGCAGCCTC (HRAS)
NM_001130442.2:c.*82_*96delinsGCGGTCAGCAGCCTC (HRAS) NP_001123914.1:n.*82_*96delinsGCGGTCAGCAGCCTC
NM_001318054.1:c.*6-32_*6-18delinsGCGGTCAGCAGCCTC (HRAS) NP_001304983.1:n.*6-32_*6-18delinsGCGGTCAGCAGCCTC
NM_005343.3:c.*6-32_*6-18delinsGCGGTCAGCAGCCTC (HRAS) NP_005334.1:n.*6-32_*6-18delinsGCGGTCAGCAGCCTC
NM_176795.4:c.*221_*235delinsGCGGTCAGCAGCCTC (HRAS) NP_789765.1:n.*221_*235delinsGCGGTCAGCAGCCTC
XM_011519875.2:c.-425+4203_-425+4217delinsGAGGCTGCTGACCGC (LRRC56) XP_011518177.1:n.-425+4203_-425+4217delinsGAGGCTGCTGACCGC
XM_011519877.2:c.-162+4203_-162+4217delinsGAGGCTGCTGACCGC (LRRC56) XP_011518179.1:n.-162+4203_-162+4217delinsGAGGCTGCTGACCGC
XM_017017167.1:c.-500+4203_-500+4217delinsGAGGCTGCTGACCGC (LRRC56) XP_016872656.1:n.-500+4203_-500+4217delinsGAGGCTGCTGACCGC
XM_017017168.1:c.-500+4203_-500+4217delinsGAGGCTGCTGACCGC (LRRC56) XP_016872657.1:n.-500+4203_-500+4217delinsGAGGCTGCTGACCGC
NM_005343.4:c.*6-32_*6-18delinsGCGGTCAGCAGCCTC (HRAS) MANE Select NP_005334.1:n.*6-32_*6-18delinsGCGGTCAGCAGCCTC
NM_001318054.2:c.*6-32_*6-18delinsGCGGTCAGCAGCCTC (HRAS) NP_001304983.1:n.*6-32_*6-18delinsGCGGTCAGCAGCCTC
NM_001130442.3:c.*82_*96delinsGCGGTCAGCAGCCTC (HRAS) NP_001123914.1:n.*82_*96delinsGCGGTCAGCAGCCTC
NM_176795.5:c.*221_*235delinsGCGGTCAGCAGCCTC (HRAS) MANE Plus Clinical NP_789765.1:n.*221_*235delinsGCGGTCAGCAGCCTC