Canonical Allele Identifier: CA16602439

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 375961
• ClinVar RCV Id: RCV000421560 ; RCV000431895 ; RCV002230756
• dbSNP Id: rs104894229
• COSMIC: COSM482 ; COSM3931342
• MyVariant Identifiers: chr11:g.534289C>G (hg19) ; chr11:g.534289C>G (hg38)
• PubMed: PMID:11150980 ; PMID:16329078 ; PMID:16443854 ; PMID:16478791 ; PMID:17054105 ; PMID:17384584 ; PMID:17412879 ; PMID:18039947 ; PMID:19255327 ; PMID:19371735 ; PMID:19382114 ; PMID:19773371 ; PMID:20660566 ; PMID:22926243 ; PMID:23406027 ; PMID:25157968

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.534289C>G , CM000673.2:g.534289C>G	GRCh38
NC_000011.9:g.534289C>G , CM000673.1:g.534289C>G	GRCh37
NC_000011.8:g.524289C>G	NCBI36
NG_007666.1:g.6262G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.34G>C (HRAS)	ENSP00000380722.3:p.Gly12Arg
ENST00000417302.7:c.34G>C (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Gly12Arg
ENST00000417302.6:c.34G>C (HRAS)	ENSP00000388246.1:p.Gly12Arg
ENST00000462734.2:c.34G>C (HRAS)	ENSP00000507303.1:p.Gly12Arg
ENST00000311189.8:c.34G>C (HRAS) MANE Select	ENSP00000309845.7:p.Gly12Arg
ENST00000311189.7:c.34G>C (HRAS)	ENSP00000309845.7:p.Gly12Arg
ENST00000397594.5:c.34G>C (HRAS)	ENSP00000380722.1:p.Gly12Arg
ENST00000397596.6:c.34G>C (HRAS)	ENSP00000380723.2:p.Gly12Arg
ENST00000417302.5:c.34G>C (HRAS)	ENSP00000388246.1:p.Gly12Arg
ENST00000451590.5:c.34G>C (HRAS)	ENSP00000407586.1:p.Gly12Arg
ENST00000468682.2:n.522G>C (HRAS)
ENST00000482021.1:n.157G>C (HRAS)
ENST00000493230.5:c.34G>C (HRAS)	ENSP00000434023.1:p.Gly12Arg
NM_001130442.1:c.34G>C (HRAS)	NP_001123914.1:p.Gly12Arg
NM_005343.2:c.34G>C (HRAS)	NP_005334.1:p.Gly12Arg
NM_176795.3:c.34G>C (HRAS)	NP_789765.1:p.Gly12Arg
XM_011519875.1:c.-424-4309C>G (LRRC56)	XP_011518177.1:n.-424-4309C>G
XM_011519877.1:c.-161-5291C>G (LRRC56)	XP_011518179.1:n.-161-5291C>G
XR_242795.1:n.233G>C (HRAS)
NM_001130442.2:c.34G>C (HRAS)	NP_001123914.1:p.Gly12Arg
NM_001318054.1:c.-286G>C (HRAS)	NP_001304983.1:n.-286G>C
NM_005343.3:c.34G>C (HRAS)	NP_005334.1:p.Gly12Arg
NM_176795.4:c.34G>C (HRAS)	NP_789765.1:p.Gly12Arg
XM_011519875.2:c.-424-4309C>G (LRRC56)	XP_011518177.1:n.-424-4309C>G
XM_011519877.2:c.-161-5291C>G (LRRC56)	XP_011518179.1:n.-161-5291C>G
XM_017017167.1:c.-499-4234C>G (LRRC56)	XP_016872656.1:n.-499-4234C>G
XM_017017168.1:c.-499-4234C>G (LRRC56)	XP_016872657.1:n.-499-4234C>G
NM_005343.4:c.34G>C (HRAS) MANE Select	NP_005334.1:p.Gly12Arg
NM_001318054.2:c.-286G>C (HRAS)	NP_001304983.1:n.-286G>C
NM_001130442.3:c.34G>C (HRAS)	NP_001123914.1:p.Gly12Arg
NM_176795.5:c.34G>C (HRAS) MANE Plus Clinical	NP_789765.1:p.Gly12Arg