Canonical Allele Identifier: CA256490

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 12605
• ClinVar RCV Id: RCV000013439 ; RCV000353386
• dbSNP Id: rs104894227
• MyVariant Identifiers: chr11:g.533553T>C (hg19) ; chr11:g.533553T>C (hg38)
• ERepo: CA256490/MONDO:0009026/004
• PubMed: PMID:16443854 ; PMID:17979197 ; PMID:21850009

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.533553T>C , CM000673.2:g.533553T>C	GRCh38
NC_000011.9:g.533553T>C , CM000673.1:g.533553T>C	GRCh37
NC_000011.8:g.523553T>C	NCBI36
NG_007666.1:g.6998A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000397594.7:c.350A>G (HRAS)	ENSP00000380722.3:p.Lys117Arg
ENST00000417302.7:c.350A>G (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Lys117Arg
ENST00000397594.6:c.68A>G (HRAS)	ENSP00000380722.2:p.Lys23Arg
ENST00000417302.6:c.350A>G (HRAS)	ENSP00000388246.1:p.Lys117Arg
ENST00000462734.2:c.350A>G (HRAS)	ENSP00000507303.1:p.Lys117Arg
ENST00000311189.8:c.350A>G (HRAS) MANE Select	ENSP00000309845.7:p.Lys117Arg
ENST00000311189.7:c.350A>G (HRAS)	ENSP00000309845.7:p.Lys117Arg
ENST00000397594.5:c.350A>G (HRAS)	ENSP00000380722.1:p.Lys117Arg
ENST00000397596.6:c.350A>G (HRAS)	ENSP00000380723.2:p.Lys117Arg
ENST00000417302.5:c.350A>G (HRAS)	ENSP00000388246.1:p.Lys117Arg
ENST00000451590.5:c.350A>G (HRAS)	ENSP00000407586.1:p.Lys117Arg
ENST00000462734.1:n.43A>G (HRAS)
ENST00000478324.5:n.60A>G (HRAS)
ENST00000479482.1:n.271A>G (HRAS)
ENST00000493230.5:c.350A>G (HRAS)	ENSP00000434023.1:p.Lys117Arg
NM_001130442.1:c.350A>G (HRAS)	NP_001123914.1:p.Lys117Arg
NM_005343.2:c.350A>G (HRAS)	NP_005334.1:p.Lys117Arg
NM_176795.3:c.350A>G (HRAS)	NP_789765.1:p.Lys117Arg
XM_011519875.1:c.-424-5045T>C (LRRC56)	XP_011518177.1:n.-424-5045T>C
XM_011519877.1:c.-162+5216T>C (LRRC56)	XP_011518179.1:n.-162+5216T>C
XR_242795.1:n.549A>G (HRAS)
NM_001130442.2:c.350A>G (HRAS)	NP_001123914.1:p.Lys117Arg
NM_001318054.1:c.31A>G (HRAS)	NP_001304983.1:p.Ser11Gly
NM_005343.3:c.350A>G (HRAS)	NP_005334.1:p.Lys117Arg
NM_176795.4:c.350A>G (HRAS)	NP_789765.1:p.Lys117Arg
XM_011519875.2:c.-424-5045T>C (LRRC56)	XP_011518177.1:n.-424-5045T>C
XM_011519877.2:c.-162+5216T>C (LRRC56)	XP_011518179.1:n.-162+5216T>C
XM_017017167.1:c.-499-4970T>C (LRRC56)	XP_016872656.1:n.-499-4970T>C
XM_017017168.1:c.-499-4970T>C (LRRC56)	XP_016872657.1:n.-499-4970T>C
NM_005343.4:c.350A>G (HRAS) MANE Select	NP_005334.1:p.Lys117Arg
NM_001318054.2:c.31A>G (HRAS)	NP_001304983.1:p.Ser11Gly
NM_001130442.3:c.350A>G (HRAS)	NP_001123914.1:p.Lys117Arg
NM_176795.5:c.350A>G (HRAS) MANE Plus Clinical	NP_789765.1:p.Lys117Arg