Canonical Allele Identifier: CA2740090852

Linked Data

ClinVar Variation Id: 3010191
ClinVar RCV Id: RCV003867366

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532731_532733delinsC , CM000673.2:g.532731_532733delinsC GRCh38
NC_000011.9:g.532731_532733delinsC , CM000673.1:g.532731_532733delinsC GRCh37
NC_000011.8:g.522731_522733delinsC NCBI36
NG_007666.1:g.7818_7820delinsG

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*20-103_*20-101delinsG (HRAS) ENSP00000380722.3:n.*20-103_*20-101delinsG
ENST00000417302.7:c.*42_*44delinsG (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*42_*44delinsG
ENST00000397594.6:c.251-103_251-101delinsG (HRAS) ENSP00000380722.2:n.251-103_251-101delinsG
ENST00000417302.6:c.*42_*44delinsG (HRAS) ENSP00000388246.1:n.*42_*44delinsG
ENST00000462734.2:c.*85_*87delinsG (HRAS) ENSP00000507303.1:n.*85_*87delinsG
ENST00000311189.8:c.473_475delinsG (HRAS) MANE Select ENSP00000309845.7:p.Thr158SerfsTer4
ENST00000311189.7:c.473_475delinsG (HRAS) ENSP00000309845.7:p.Thr158SerfsTer4
ENST00000397594.5:c.*42_*44delinsG (HRAS) ENSP00000380722.1:n.*42_*44delinsG
ENST00000397596.6:c.473_475delinsG (HRAS) ENSP00000380723.2:p.Thr158SerfsTer4
ENST00000417302.5:c.*42_*44delinsG (HRAS) ENSP00000388246.1:n.*42_*44delinsG
ENST00000451590.5:c.473_475delinsG (HRAS) ENSP00000407586.1:p.Thr158SerfsTer4
ENST00000462734.1:n.248_250delinsG (HRAS)
ENST00000478324.5:n.243-103_243-101delinsG (HRAS)
ENST00000479482.1:n.394_396delinsG (HRAS)
ENST00000493230.5:c.*42_*44delinsG (HRAS) ENSP00000434023.1:n.*42_*44delinsG
NM_001130442.1:c.473_475delinsG (HRAS) NP_001123914.1:p.Thr158SerfsTer4
NM_005343.2:c.473_475delinsG (HRAS) NP_005334.1:p.Thr158SerfsTer4
NM_176795.3:c.*42_*44delinsG (HRAS) NP_789765.1:n.*42_*44delinsG
XM_011519875.1:c.-425+4394_-425+4396delinsC (LRRC56) XP_011518177.1:n.-425+4394_-425+4396delinsC
XM_011519877.1:c.-162+4394_-162+4396delinsC (LRRC56) XP_011518179.1:n.-162+4394_-162+4396delinsC
XR_242795.1:n.754_756delinsG (HRAS)
NM_001130442.2:c.473_475delinsG (HRAS) NP_001123914.1:p.Thr158SerfsTer4
NM_001318054.1:c.236_238delinsG (HRAS) NP_001304983.1:p.Thr79SerfsTer4
NM_005343.3:c.473_475delinsG (HRAS) NP_005334.1:p.Thr158SerfsTer4
NM_176795.4:c.*42_*44delinsG (HRAS) NP_789765.1:n.*42_*44delinsG
XM_011519875.2:c.-425+4394_-425+4396delinsC (LRRC56) XP_011518177.1:n.-425+4394_-425+4396delinsC
XM_011519877.2:c.-162+4394_-162+4396delinsC (LRRC56) XP_011518179.1:n.-162+4394_-162+4396delinsC
XM_017017167.1:c.-500+4394_-500+4396delinsC (LRRC56) XP_016872656.1:n.-500+4394_-500+4396delinsC
XM_017017168.1:c.-500+4394_-500+4396delinsC (LRRC56) XP_016872657.1:n.-500+4394_-500+4396delinsC
NM_005343.4:c.473_475delinsG (HRAS) MANE Select NP_005334.1:p.Thr158SerfsTer4
NM_001318054.2:c.236_238delinsG (HRAS) NP_001304983.1:p.Thr79SerfsTer4
NM_001130442.3:c.473_475delinsG (HRAS) NP_001123914.1:p.Thr158SerfsTer4
NM_176795.5:c.*42_*44delinsG (HRAS) MANE Plus Clinical NP_789765.1:n.*42_*44delinsG