Canonical Allele Identifier: CA5779312

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 936167
• ClinVar RCV Id: RCV001204909
• dbSNP Id: rs533567288
• ExAC: 11:533477 G / C
• gnomAD v2: 11-533477-G-C
• gnomAD v4: 11-533477-G-C
• MyVariant Identifiers: chr11:g.533477G>C (hg19) ; chr11:g.533477G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.533477G>C , CM000673.2:g.533477G>C	GRCh38
NC_000011.9:g.533477G>C , CM000673.1:g.533477G>C	GRCh37
NC_000011.8:g.523477G>C	NCBI36
NG_007666.1:g.7074C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000397594.7:c.426C>G (HRAS)	ENSP00000380722.3:p.Ile142Met
ENST00000417302.7:c.426C>G (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Ile142Met
ENST00000397594.6:c.144C>G (HRAS)	ENSP00000380722.2:p.Ile48Met
ENST00000417302.6:c.426C>G (HRAS)	ENSP00000388246.1:p.Ile142Met
ENST00000462734.2:c.426C>G (HRAS)	ENSP00000507303.1:p.Ile142Met
ENST00000311189.8:c.426C>G (HRAS) MANE Select	ENSP00000309845.7:p.Ile142Met
ENST00000311189.7:c.426C>G (HRAS)	ENSP00000309845.7:p.Ile142Met
ENST00000397594.5:c.426C>G (HRAS)	ENSP00000380722.1:p.Ile142Met
ENST00000397596.6:c.426C>G (HRAS)	ENSP00000380723.2:p.Ile142Met
ENST00000417302.5:c.426C>G (HRAS)	ENSP00000388246.1:p.Ile142Met
ENST00000451590.5:c.426C>G (HRAS)	ENSP00000407586.1:p.Ile142Met
ENST00000462734.1:n.119C>G (HRAS)
ENST00000478324.5:n.136C>G (HRAS)
ENST00000479482.1:n.347C>G (HRAS)
ENST00000493230.5:c.426C>G (HRAS)	ENSP00000434023.1:p.Ile142Met
NM_001130442.1:c.426C>G (HRAS)	NP_001123914.1:p.Ile142Met
NM_005343.2:c.426C>G (HRAS)	NP_005334.1:p.Ile142Met
NM_176795.3:c.426C>G (HRAS)	NP_789765.1:p.Ile142Met
XM_011519875.1:c.-424-5121G>C (LRRC56)	XP_011518177.1:n.-424-5121G>C
XM_011519877.1:c.-162+5140G>C (LRRC56)	XP_011518179.1:n.-162+5140G>C
XR_242795.1:n.625C>G (HRAS)
NM_001130442.2:c.426C>G (HRAS)	NP_001123914.1:p.Ile142Met
NM_001318054.1:c.107C>G (HRAS)	NP_001304983.1:p.Ser36Trp
NM_005343.3:c.426C>G (HRAS)	NP_005334.1:p.Ile142Met
NM_176795.4:c.426C>G (HRAS)	NP_789765.1:p.Ile142Met
XM_011519875.2:c.-424-5121G>C (LRRC56)	XP_011518177.1:n.-424-5121G>C
XM_011519877.2:c.-162+5140G>C (LRRC56)	XP_011518179.1:n.-162+5140G>C
XM_017017167.1:c.-499-5046G>C (LRRC56)	XP_016872656.1:n.-499-5046G>C
XM_017017168.1:c.-499-5046G>C (LRRC56)	XP_016872657.1:n.-499-5046G>C
NM_005343.4:c.426C>G (HRAS) MANE Select	NP_005334.1:p.Ile142Met
NM_001318054.2:c.107C>G (HRAS)	NP_001304983.1:p.Ser36Trp
NM_001130442.3:c.426C>G (HRAS)	NP_001123914.1:p.Ile142Met
NM_176795.5:c.426C>G (HRAS) MANE Plus Clinical	NP_789765.1:p.Ile142Met