Canonical Allele Identifier: CA2573147054

Linked Data

ClinVar Variation Id: 1691376
ClinVar RCV Id: RCV002254474
dbSNP Id: rs2133990531

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.533836_533865dup , CM000673.2:g.533836_533865dup GRCh38
NC_000011.9:g.533836_533865dup , CM000673.1:g.533836_533865dup GRCh37
NC_000011.8:g.523836_523865dup NCBI36
NG_007666.1:g.6686_6715dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.191_220dup (HRAS) ENSP00000380722.3:p.Arg73_Thr74insAsnSerAlaMetArgAspGlnTyrMet...
ENST00000417302.7:c.191_220dup (HRAS) MANE Plus Clinical ENSP00000388246.1:p.Arg73_Thr74insAsnSerAlaMetArgAspGlnTyrMet...
ENST00000417302.6:c.191_220dup (HRAS) ENSP00000388246.1:p.Arg73_Thr74insAsnSerAlaMetArgAspGlnTyrMet...
ENST00000462734.2:c.191_220dup (HRAS) ENSP00000507303.1:p.Arg73_Thr74insAsnSerAlaMetArgAspGlnTyrMet...
ENST00000311189.8:c.191_220dup (HRAS) MANE Select ENSP00000309845.7:p.Arg73_Thr74insAsnSerAlaMetArgAspGlnTyrMet...
ENST00000311189.7:c.191_220dup (HRAS) ENSP00000309845.7:p.Arg73_Thr74insAsnSerAlaMetArgAspGlnTyrMet...
ENST00000397594.5:c.191_220dup (HRAS) ENSP00000380722.1:p.Arg73_Thr74insAsnSerAlaMetArgAspGlnTyrMet...
ENST00000397596.6:c.191_220dup (HRAS) ENSP00000380723.2:p.Arg73_Thr74insAsnSerAlaMetArgAspGlnTyrMet...
ENST00000417302.5:c.191_220dup (HRAS) ENSP00000388246.1:p.Arg73_Thr74insAsnSerAlaMetArgAspGlnTyrMet...
ENST00000451590.5:c.191_220dup (HRAS) ENSP00000407586.1:p.Arg73_Thr74insAsnSerAlaMetArgAspGlnTyrMet...
ENST00000468682.2:n.679_708dup (HRAS)
ENST00000479482.1:n.112_141dup (HRAS)
ENST00000493230.5:c.191_220dup (HRAS) ENSP00000434023.1:p.Arg73_Thr74insAsnSerAlaMetArgAspGlnTyrMet...
NM_001130442.1:c.191_220dup (HRAS) NP_001123914.1:p.Arg73_Thr74insAsnSerAlaMetArgAspGlnTyrMetArg...
NM_005343.2:c.191_220dup (HRAS) NP_005334.1:p.Arg73_Thr74insAsnSerAlaMetArgAspGlnTyrMetArg
NM_176795.3:c.191_220dup (HRAS) NP_789765.1:p.Arg73_Thr74insAsnSerAlaMetArgAspGlnTyrMetArg
XM_011519875.1:c.-424-4762_-424-4733dup (LRRC56) XP_011518177.1:n.-424-4762_-424-4733dup
XM_011519877.1:c.-162+5499_-162+5528dup (LRRC56) XP_011518179.1:n.-162+5499_-162+5528dup
XR_242795.1:n.390_419dup (HRAS)
NM_001130442.2:c.191_220dup (HRAS) NP_001123914.1:p.Arg73_Thr74insAsnSerAlaMetArgAspGlnTyrMetArg...
NM_001318054.1:c.-129_-100dup (HRAS) NP_001304983.1:n.-129_-100dup
NM_005343.3:c.191_220dup (HRAS) NP_005334.1:p.Arg73_Thr74insAsnSerAlaMetArgAspGlnTyrMetArg
NM_176795.4:c.191_220dup (HRAS) NP_789765.1:p.Arg73_Thr74insAsnSerAlaMetArgAspGlnTyrMetArg
XM_011519875.2:c.-424-4762_-424-4733dup (LRRC56) XP_011518177.1:n.-424-4762_-424-4733dup
XM_011519877.2:c.-162+5499_-162+5528dup (LRRC56) XP_011518179.1:n.-162+5499_-162+5528dup
XM_017017167.1:c.-499-4687_-499-4658dup (LRRC56) XP_016872656.1:n.-499-4687_-499-4658dup
XM_017017168.1:c.-499-4687_-499-4658dup (LRRC56) XP_016872657.1:n.-499-4687_-499-4658dup
NM_005343.4:c.191_220dup (HRAS) MANE Select NP_005334.1:p.Arg73_Thr74insAsnSerAlaMetArgAspGlnTyrMetArg
NM_001318054.2:c.-129_-100dup (HRAS) NP_001304983.1:n.-129_-100dup
NM_001130442.3:c.191_220dup (HRAS) NP_001123914.1:p.Arg73_Thr74insAsnSerAlaMetArgAspGlnTyrMetArg...
NM_176795.5:c.191_220dup (HRAS) MANE Plus Clinical NP_789765.1:p.Arg73_Thr74insAsnSerAlaMetArgAspGlnTyrMetArg