Canonical Allele Identifier: CA677772757
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

dbSNP Id: rs1278915826
MyVariant Identifiers: chr11:g.532490C>G (hg19) chr11:g.532490C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532490C>G , CM000673.2:g.532490C>G GRCh38
NC_000011.9:g.532490C>G , CM000673.1:g.532490C>G GRCh37
NC_000011.8:g.522490C>G NCBI36
NG_007666.1:g.8061G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*160G>C (HRAS) ENSP00000380722.3:n.*160G>C
ENST00000417302.7:c.*285G>C (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*285G>C
ENST00000397594.6:c.391G>C (HRAS) ENSP00000380722.2:n.391G>C
ENST00000417302.6:c.*285G>C (HRAS) ENSP00000388246.1:n.*285G>C
ENST00000462734.2:c.*220G>C (HRAS) ENSP00000507303.1:n.*220G>C
ENST00000311189.8:c.*38G>C (HRAS) MANE Select ENSP00000309845.7:n.*38G>C
ENST00000311189.7:c.*38G>C (HRAS) ENSP00000309845.7:n.*38G>C
ENST00000397594.5:c.*285G>C (HRAS) ENSP00000380722.1:n.*285G>C
ENST00000397596.6:c.*146G>C (HRAS) ENSP00000380723.2:n.*146G>C
ENST00000417302.5:c.*285G>C (HRAS) ENSP00000388246.1:n.*285G>C
ENST00000451590.5:c.*146G>C (HRAS) ENSP00000407586.1:n.*146G>C
ENST00000462734.1:n.383G>C (HRAS)
ENST00000478324.5:n.383G>C (HRAS)
ENST00000493230.5:c.*177G>C (HRAS) ENSP00000434023.1:n.*177G>C
NM_001130442.1:c.*146G>C (HRAS) NP_001123914.1:n.*146G>C
NM_005343.2:c.*38G>C (HRAS) NP_005334.1:n.*38G>C
NM_176795.3:c.*285G>C (HRAS) NP_789765.1:n.*285G>C
XM_011519875.1:c.-425+4153C>G (LRRC56) XP_011518177.1:n.-425+4153C>G
XM_011519877.1:c.-162+4153C>G (LRRC56) XP_011518179.1:n.-162+4153C>G
XR_242795.1:n.889G>C (HRAS)
NM_001130442.2:c.*146G>C (HRAS) NP_001123914.1:n.*146G>C
NM_001318054.1:c.*38G>C (HRAS) NP_001304983.1:n.*38G>C
NM_005343.3:c.*38G>C (HRAS) NP_005334.1:n.*38G>C
NM_176795.4:c.*285G>C (HRAS) NP_789765.1:n.*285G>C
XM_011519875.2:c.-425+4153C>G (LRRC56) XP_011518177.1:n.-425+4153C>G
XM_011519877.2:c.-162+4153C>G (LRRC56) XP_011518179.1:n.-162+4153C>G
XM_017017167.1:c.-500+4153C>G (LRRC56) XP_016872656.1:n.-500+4153C>G
XM_017017168.1:c.-500+4153C>G (LRRC56) XP_016872657.1:n.-500+4153C>G
NM_005343.4:c.*38G>C (HRAS) MANE Select NP_005334.1:n.*38G>C
NM_001318054.2:c.*38G>C (HRAS) NP_001304983.1:n.*38G>C
NM_001130442.3:c.*146G>C (HRAS) NP_001123914.1:n.*146G>C
NM_176795.5:c.*285G>C (HRAS) MANE Plus Clinical NP_789765.1:n.*285G>C
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