Canonical Allele Identifier: CA378921170
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

ClinVar Variation Id: 1692890
ClinVar RCV Id: RCV002258705
dbSNP Id: rs758956556
MyVariant Identifiers: chr11:g.532725G>C (hg19) chr11:g.532725G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532725G>C , CM000673.2:g.532725G>C GRCh38
NC_000011.9:g.532725G>C , CM000673.1:g.532725G>C GRCh37
NC_000011.8:g.522725G>C NCBI36
NG_007666.1:g.7826C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*20-95C>G (HRAS) ENSP00000380722.3:n.*20-95C>G
ENST00000417302.7:c.*50C>G (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*50C>G
ENST00000397594.6:c.251-95C>G (HRAS) ENSP00000380722.2:n.251-95C>G
ENST00000417302.6:c.*50C>G (HRAS) ENSP00000388246.1:n.*50C>G
ENST00000462734.2:c.*93C>G (HRAS) ENSP00000507303.1:n.*93C>G
ENST00000311189.8:c.481C>G (HRAS) MANE Select ENSP00000309845.7:p.Arg161Gly
ENST00000311189.7:c.481C>G (HRAS) ENSP00000309845.7:p.Arg161Gly
ENST00000397594.5:c.*50C>G (HRAS) ENSP00000380722.1:n.*50C>G
ENST00000397596.6:c.481C>G (HRAS) ENSP00000380723.2:p.Arg161Gly
ENST00000417302.5:c.*50C>G (HRAS) ENSP00000388246.1:n.*50C>G
ENST00000451590.5:c.481C>G (HRAS) ENSP00000407586.1:p.Arg161Gly
ENST00000462734.1:n.256C>G (HRAS)
ENST00000478324.5:n.243-95C>G (HRAS)
ENST00000479482.1:n.402C>G (HRAS)
ENST00000493230.5:c.*50C>G (HRAS) ENSP00000434023.1:n.*50C>G
NM_001130442.1:c.481C>G (HRAS) NP_001123914.1:p.Arg161Gly
NM_005343.2:c.481C>G (HRAS) NP_005334.1:p.Arg161Gly
NM_176795.3:c.*50C>G (HRAS) NP_789765.1:n.*50C>G
XM_011519875.1:c.-425+4388G>C (LRRC56) XP_011518177.1:n.-425+4388G>C
XM_011519877.1:c.-162+4388G>C (LRRC56) XP_011518179.1:n.-162+4388G>C
XR_242795.1:n.762C>G (HRAS)
NM_001130442.2:c.481C>G (HRAS) NP_001123914.1:p.Arg161Gly
NM_001318054.1:c.244C>G (HRAS) NP_001304983.1:p.Arg82Gly
NM_005343.3:c.481C>G (HRAS) NP_005334.1:p.Arg161Gly
NM_176795.4:c.*50C>G (HRAS) NP_789765.1:n.*50C>G
XM_011519875.2:c.-425+4388G>C (LRRC56) XP_011518177.1:n.-425+4388G>C
XM_011519877.2:c.-162+4388G>C (LRRC56) XP_011518179.1:n.-162+4388G>C
XM_017017167.1:c.-500+4388G>C (LRRC56) XP_016872656.1:n.-500+4388G>C
XM_017017168.1:c.-500+4388G>C (LRRC56) XP_016872657.1:n.-500+4388G>C
NM_005343.4:c.481C>G (HRAS) MANE Select NP_005334.1:p.Arg161Gly
NM_001318054.2:c.244C>G (HRAS) NP_001304983.1:p.Arg82Gly
NM_001130442.3:c.481C>G (HRAS) NP_001123914.1:p.Arg161Gly
NM_176795.5:c.*50C>G (HRAS) MANE Plus Clinical NP_789765.1:n.*50C>G
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