This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: CA1947141864
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.533115A= , CM000673.2:g.533115A= GRCh38
NC_000011.9:g.533115A= , CM000673.1:g.533115A= GRCh37
NC_000011.8:g.523115A= NCBI36
NG_007666.1:g.7436T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*19+162T= (HRAS) ENSP00000380722.3:n.*19+162T=
ENST00000417302.7:c.*19+162T= (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*19+162T=
ENST00000397594.6:c.250+162T= (HRAS) ENSP00000380722.2:n.250+162T=
ENST00000417302.6:c.*19+162T= (HRAS) ENSP00000388246.1:n.*19+162T=
ENST00000462734.2:c.*62+162T= (HRAS) ENSP00000507303.1:n.*62+162T=
ENST00000311189.8:c.450+338T= (HRAS) MANE Select ENSP00000309845.7:n.450+338T=
ENST00000311189.7:c.450+338T= (HRAS) ENSP00000309845.7:n.450+338T=
ENST00000397594.5:c.*19+162T= (HRAS) ENSP00000380722.1:n.*19+162T=
ENST00000397596.6:c.450+338T= (HRAS) ENSP00000380723.2:n.450+338T=
ENST00000417302.5:c.*19+162T= (HRAS) ENSP00000388246.1:n.*19+162T=
ENST00000451590.5:c.450+338T= (HRAS) ENSP00000407586.1:n.450+338T=
ENST00000462734.1:n.225+162T= (HRAS)
ENST00000478324.5:n.242+162T= (HRAS)
ENST00000479482.1:n.371+338T= (HRAS)
ENST00000493230.5:c.*19+162T= (HRAS) ENSP00000434023.1:n.*19+162T=
NM_001130442.1:c.450+338T= (HRAS) NP_001123914.1:n.450+338T=
NM_005343.2:c.450+338T= (HRAS) NP_005334.1:n.450+338T=
NM_176795.3:c.*19+162T= (HRAS) NP_789765.1:n.*19+162T=
XM_011519875.1:c.-425+4778A= (LRRC56) XP_011518177.1:n.-425+4778A=
XM_011519877.1:c.-162+4778A= (LRRC56) XP_011518179.1:n.-162+4778A=
XR_242795.1:n.731+162T= (HRAS)
NM_001130442.2:c.450+338T= (HRAS) NP_001123914.1:n.450+338T=
NM_001318054.1:c.213+162T= (HRAS) NP_001304983.1:n.213+162T=
NM_005343.3:c.450+338T= (HRAS) NP_005334.1:n.450+338T=
NM_176795.4:c.*19+162T= (HRAS) NP_789765.1:n.*19+162T=
XM_011519875.2:c.-425+4778A= (LRRC56) XP_011518177.1:n.-425+4778A=
XM_011519877.2:c.-162+4778A= (LRRC56) XP_011518179.1:n.-162+4778A=
XM_017017167.1:c.-500+4778A= (LRRC56) XP_016872656.1:n.-500+4778A=
XM_017017168.1:c.-500+4778A= (LRRC56) XP_016872657.1:n.-500+4778A=
NM_005343.4:c.450+338T= (HRAS) MANE Select NP_005334.1:n.450+338T=
NM_001318054.2:c.213+162T= (HRAS) NP_001304983.1:n.213+162T=
NM_001130442.3:c.450+338T= (HRAS) NP_001123914.1:n.450+338T=
NM_176795.5:c.*19+162T= (HRAS) MANE Plus Clinical NP_789765.1:n.*19+162T=
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