Canonical Allele Identifier: CA378924704
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

dbSNP Id: rs1261188136
MyVariant Identifiers: chr11:g.533891G>C (hg19) chr11:g.533891G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.533891G>C , CM000673.2:g.533891G>C GRCh38
NC_000011.9:g.533891G>C , CM000673.1:g.533891G>C GRCh37
NC_000011.8:g.523891G>C NCBI36
NG_007666.1:g.6660C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.165C>G (HRAS) ENSP00000380722.3:p.Ile55Met
ENST00000417302.7:c.165C>G (HRAS) MANE Plus Clinical ENSP00000388246.1:p.Ile55Met
ENST00000417302.6:c.165C>G (HRAS) ENSP00000388246.1:p.Ile55Met
ENST00000462734.2:c.165C>G (HRAS) ENSP00000507303.1:p.Ile55Met
ENST00000311189.8:c.165C>G (HRAS) MANE Select ENSP00000309845.7:p.Ile55Met
ENST00000311189.7:c.165C>G (HRAS) ENSP00000309845.7:p.Ile55Met
ENST00000397594.5:c.165C>G (HRAS) ENSP00000380722.1:p.Ile55Met
ENST00000397596.6:c.165C>G (HRAS) ENSP00000380723.2:p.Ile55Met
ENST00000417302.5:c.165C>G (HRAS) ENSP00000388246.1:p.Ile55Met
ENST00000451590.5:c.165C>G (HRAS) ENSP00000407586.1:p.Ile55Met
ENST00000468682.2:n.653C>G (HRAS)
ENST00000479482.1:n.86C>G (HRAS)
ENST00000493230.5:c.165C>G (HRAS) ENSP00000434023.1:p.Ile55Met
NM_001130442.1:c.165C>G (HRAS) NP_001123914.1:p.Ile55Met
NM_005343.2:c.165C>G (HRAS) NP_005334.1:p.Ile55Met
NM_176795.3:c.165C>G (HRAS) NP_789765.1:p.Ile55Met
XM_011519875.1:c.-424-4707G>C (LRRC56) XP_011518177.1:n.-424-4707G>C
XM_011519877.1:c.-162+5554G>C (LRRC56) XP_011518179.1:n.-162+5554G>C
XR_242795.1:n.364C>G (HRAS)
NM_001130442.2:c.165C>G (HRAS) NP_001123914.1:p.Ile55Met
NM_001318054.1:c.-155C>G (HRAS) NP_001304983.1:n.-155C>G
NM_005343.3:c.165C>G (HRAS) NP_005334.1:p.Ile55Met
NM_176795.4:c.165C>G (HRAS) NP_789765.1:p.Ile55Met
XM_011519875.2:c.-424-4707G>C (LRRC56) XP_011518177.1:n.-424-4707G>C
XM_011519877.2:c.-162+5554G>C (LRRC56) XP_011518179.1:n.-162+5554G>C
XM_017017167.1:c.-499-4632G>C (LRRC56) XP_016872656.1:n.-499-4632G>C
XM_017017168.1:c.-499-4632G>C (LRRC56) XP_016872657.1:n.-499-4632G>C
NM_005343.4:c.165C>G (HRAS) MANE Select NP_005334.1:p.Ile55Met
NM_001318054.2:c.-155C>G (HRAS) NP_001304983.1:n.-155C>G
NM_001130442.3:c.165C>G (HRAS) NP_001123914.1:p.Ile55Met
NM_176795.5:c.165C>G (HRAS) MANE Plus Clinical NP_789765.1:p.Ile55Met
Search 100 bp 5'
Search 100 bp 3'