Canonical Allele Identifier: CA5779217
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

dbSNP Id: rs766474932
ExAC: 11:532704 G / C
gnomAD v2: 11-532704-G-C
MyVariant Identifiers: chr11:g.532704G>C (hg19) chr11:g.532704G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532704G>C , CM000673.2:g.532704G>C GRCh38
NC_000011.9:g.532704G>C , CM000673.1:g.532704G>C GRCh37
NC_000011.8:g.522704G>C NCBI36
NG_007666.1:g.7847C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*20-74C>G (HRAS) ENSP00000380722.3:n.*20-74C>G
ENST00000417302.7:c.*71C>G (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*71C>G
ENST00000397594.6:c.251-74C>G (HRAS) ENSP00000380722.2:n.251-74C>G
ENST00000417302.6:c.*71C>G (HRAS) ENSP00000388246.1:n.*71C>G
ENST00000462734.2:c.*114C>G (HRAS) ENSP00000507303.1:n.*114C>G
ENST00000311189.8:c.502C>G (HRAS) MANE Select ENSP00000309845.7:p.Leu168Val
ENST00000311189.7:c.502C>G (HRAS) ENSP00000309845.7:p.Leu168Val
ENST00000397594.5:c.*71C>G (HRAS) ENSP00000380722.1:n.*71C>G
ENST00000397596.6:c.502C>G (HRAS) ENSP00000380723.2:p.Leu168Val
ENST00000417302.5:c.*71C>G (HRAS) ENSP00000388246.1:n.*71C>G
ENST00000451590.5:c.502C>G (HRAS) ENSP00000407586.1:p.Leu168Val
ENST00000462734.1:n.277C>G (HRAS)
ENST00000478324.5:n.243-74C>G (HRAS)
ENST00000479482.1:n.423C>G (HRAS)
ENST00000493230.5:c.*71C>G (HRAS) ENSP00000434023.1:n.*71C>G
NM_001130442.1:c.502C>G (HRAS) NP_001123914.1:p.Leu168Val
NM_005343.2:c.502C>G (HRAS) NP_005334.1:p.Leu168Val
NM_176795.3:c.*71C>G (HRAS) NP_789765.1:n.*71C>G
XM_011519875.1:c.-425+4367G>C (LRRC56) XP_011518177.1:n.-425+4367G>C
XM_011519877.1:c.-162+4367G>C (LRRC56) XP_011518179.1:n.-162+4367G>C
XR_242795.1:n.783C>G (HRAS)
NM_001130442.2:c.502C>G (HRAS) NP_001123914.1:p.Leu168Val
NM_001318054.1:c.265C>G (HRAS) NP_001304983.1:p.Leu89Val
NM_005343.3:c.502C>G (HRAS) NP_005334.1:p.Leu168Val
NM_176795.4:c.*71C>G (HRAS) NP_789765.1:n.*71C>G
XM_011519875.2:c.-425+4367G>C (LRRC56) XP_011518177.1:n.-425+4367G>C
XM_011519877.2:c.-162+4367G>C (LRRC56) XP_011518179.1:n.-162+4367G>C
XM_017017167.1:c.-500+4367G>C (LRRC56) XP_016872656.1:n.-500+4367G>C
XM_017017168.1:c.-500+4367G>C (LRRC56) XP_016872657.1:n.-500+4367G>C
NM_005343.4:c.502C>G (HRAS) MANE Select NP_005334.1:p.Leu168Val
NM_001318054.2:c.265C>G (HRAS) NP_001304983.1:p.Leu89Val
NM_001130442.3:c.502C>G (HRAS) NP_001123914.1:p.Leu168Val
NM_176795.5:c.*71C>G (HRAS) MANE Plus Clinical NP_789765.1:n.*71C>G
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