Canonical Allele Identifier: CA122549

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 12602
• ClinVar RCV Id: RCV000013436 ; RCV000013435 ; RCV000022796 ; RCV000029209 ; RCV000081295 ; RCV000149828 ; RCV000417494 ; RCV000422253 ; RCV000425542 ; RCV000430725 ; RCV000432342 ; RCV000433576 ; RCV000432945 ; RCV000438022 ; RCV000440297 ; RCV000443940 ; RCV000430608 ; RCV000419709 ; RCV000420366 ; RCV000435163 ; RCV000422656 ; RCV000423310 ; RCV000424896 ; RCV000440863 ; RCV000440993 ; RCV000445039 ; RCV000427772 ; RCV000430011 ; RCV000432984 ; RCV000440237 ; RCV000487471 ; RCV001257537 ; RCV001255689 ; RCV001813185 ; RCV003156059 ; RCV003398496 ; RCV002453256 ; RCV003450635 ; RCV003450636
• dbSNP Id: rs104894229
• COSMIC: COSM480 ; COSM1746299
• MyVariant Identifiers: chr11:g.534289C>T (hg19) ; chr11:g.534289C>T (hg38)
• ERepo: CA122549/MONDO:0009026/004
• PubMed: PMID:11150980 ; PMID:16170316 ; PMID:16329078 ; PMID:16372351 ; PMID:16443854 ; PMID:16835863 ; PMID:16881968 ; PMID:16969868 ; PMID:17054105 ; PMID:17412879 ; PMID:18039947 ; PMID:18978862 ; PMID:19206176 ; PMID:19371735 ; PMID:19382114 ; PMID:19669404 ; PMID:20660566 ; PMID:21850009 ; PMID:22926243 ; PMID:23891399 ; PMID:26619011

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.34G>A (HRAS)	ENSP00000380722.3:p.Gly12Ser
ENST00000417302.7:c.34G>A (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Gly12Ser
ENST00000417302.6:c.34G>A (HRAS)	ENSP00000388246.1:p.Gly12Ser
ENST00000462734.2:c.34G>A (HRAS)	ENSP00000507303.1:p.Gly12Ser
ENST00000311189.8:c.34G>A (HRAS) MANE Select	ENSP00000309845.7:p.Gly12Ser
ENST00000311189.7:c.34G>A (HRAS)	ENSP00000309845.7:p.Gly12Ser
ENST00000397594.5:c.34G>A (HRAS)	ENSP00000380722.1:p.Gly12Ser
ENST00000397596.6:c.34G>A (HRAS)	ENSP00000380723.2:p.Gly12Ser
ENST00000417302.5:c.34G>A (HRAS)	ENSP00000388246.1:p.Gly12Ser
ENST00000451590.5:c.34G>A (HRAS)	ENSP00000407586.1:p.Gly12Ser
ENST00000468682.2:n.522G>A (HRAS)
ENST00000482021.1:n.157G>A (HRAS)
ENST00000493230.5:c.34G>A (HRAS)	ENSP00000434023.1:p.Gly12Ser
NM_001130442.1:c.34G>A (HRAS)	NP_001123914.1:p.Gly12Ser
NM_005343.2:c.34G>A (HRAS)	NP_005334.1:p.Gly12Ser
NM_176795.3:c.34G>A (HRAS)	NP_789765.1:p.Gly12Ser
XM_011519875.1:c.-424-4309C>T (LRRC56)	XP_011518177.1:n.-424-4309C>T
XM_011519877.1:c.-161-5291C>T (LRRC56)	XP_011518179.1:n.-161-5291C>T
XR_242795.1:n.233G>A (HRAS)
NM_001130442.2:c.34G>A (HRAS)	NP_001123914.1:p.Gly12Ser
NM_001318054.1:c.-286G>A (HRAS)	NP_001304983.1:n.-286G>A
NM_005343.3:c.34G>A (HRAS)	NP_005334.1:p.Gly12Ser
NM_176795.4:c.34G>A (HRAS)	NP_789765.1:p.Gly12Ser
XM_011519875.2:c.-424-4309C>T (LRRC56)	XP_011518177.1:n.-424-4309C>T
XM_011519877.2:c.-161-5291C>T (LRRC56)	XP_011518179.1:n.-161-5291C>T
XM_017017167.1:c.-499-4234C>T (LRRC56)	XP_016872656.1:n.-499-4234C>T
XM_017017168.1:c.-499-4234C>T (LRRC56)	XP_016872657.1:n.-499-4234C>T
NM_005343.4:c.34G>A (HRAS) MANE Select	NP_005334.1:p.Gly12Ser
NM_001318054.2:c.-286G>A (HRAS)	NP_001304983.1:n.-286G>A
NM_001130442.3:c.34G>A (HRAS)	NP_001123914.1:p.Gly12Ser
NM_176795.5:c.34G>A (HRAS) MANE Plus Clinical	NP_789765.1:p.Gly12Ser