Canonical Allele Identifier: CA256486

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 12603
• ClinVar RCV Id: RCV000013437 ; RCV000418547 ; RCV000422263 ; RCV000430806 ; RCV000417508 ; RCV000435619 ; RCV000423413 ; RCV000423622 ; RCV000207503 ; RCV000440663 ; RCV000425989 ; RCV000426130 ; RCV000428375 ; RCV000441501 ; RCV000444092 ; RCV000433266 ; RCV000445257 ; RCV000428172 ; RCV000433587 ; RCV000423741 ; RCV000425511 ; RCV000623953 ; RCV000432956 ; RCV000762848 ; RCV000435805 ; RCV000436832 ; RCV000442448 ; RCV000445090 ; RCV001813186 ; RCV001257536
• dbSNP Id: rs104894230
• COSMIC: COSM485 ; COSM120919
• MyVariant Identifiers: chr11:g.534288C>G (hg19) ; chr11:g.534288C>G (hg38)
• PubMed: PMID:6092966 ; PMID:6330729 ; PMID:12210337 ; PMID:14608654 ; PMID:16155195 ; PMID:16170316 ; PMID:16443854 ; PMID:17250658 ; PMID:17412879 ; PMID:17979197 ; PMID:18039947 ; PMID:18470943 ; PMID:20658932 ; PMID:21344638 ; PMID:21850009 ; PMID:22317973 ; PMID:22499344 ; PMID:24169525 ; PMID:26619011 ; PMID:27195699 ; PMID:27589201 ; PMID:28390077 ; PMID:29073591

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.534288C>G , CM000673.2:g.534288C>G	GRCh38
NC_000011.9:g.534288C>G , CM000673.1:g.534288C>G	GRCh37
NC_000011.8:g.524288C>G	NCBI36
NG_007666.1:g.6263G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.35G>C (HRAS)	ENSP00000380722.3:p.Gly12Ala
ENST00000417302.7:c.35G>C (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Gly12Ala
ENST00000417302.6:c.35G>C (HRAS)	ENSP00000388246.1:p.Gly12Ala
ENST00000462734.2:c.35G>C (HRAS)	ENSP00000507303.1:p.Gly12Ala
ENST00000311189.8:c.35G>C (HRAS) MANE Select	ENSP00000309845.7:p.Gly12Ala
ENST00000311189.7:c.35G>C (HRAS)	ENSP00000309845.7:p.Gly12Ala
ENST00000397594.5:c.35G>C (HRAS)	ENSP00000380722.1:p.Gly12Ala
ENST00000397596.6:c.35G>C (HRAS)	ENSP00000380723.2:p.Gly12Ala
ENST00000417302.5:c.35G>C (HRAS)	ENSP00000388246.1:p.Gly12Ala
ENST00000451590.5:c.35G>C (HRAS)	ENSP00000407586.1:p.Gly12Ala
ENST00000468682.2:n.523G>C (HRAS)
ENST00000482021.1:n.158G>C (HRAS)
ENST00000493230.5:c.35G>C (HRAS)	ENSP00000434023.1:p.Gly12Ala
NM_001130442.1:c.35G>C (HRAS)	NP_001123914.1:p.Gly12Ala
NM_005343.2:c.35G>C (HRAS)	NP_005334.1:p.Gly12Ala
NM_176795.3:c.35G>C (HRAS)	NP_789765.1:p.Gly12Ala
XM_011519875.1:c.-424-4310C>G (LRRC56)	XP_011518177.1:n.-424-4310C>G
XM_011519877.1:c.-161-5292C>G (LRRC56)	XP_011518179.1:n.-161-5292C>G
XR_242795.1:n.234G>C (HRAS)
NM_001130442.2:c.35G>C (HRAS)	NP_001123914.1:p.Gly12Ala
NM_001318054.1:c.-285G>C (HRAS)	NP_001304983.1:n.-285G>C
NM_005343.3:c.35G>C (HRAS)	NP_005334.1:p.Gly12Ala
NM_176795.4:c.35G>C (HRAS)	NP_789765.1:p.Gly12Ala
XM_011519875.2:c.-424-4310C>G (LRRC56)	XP_011518177.1:n.-424-4310C>G
XM_011519877.2:c.-161-5292C>G (LRRC56)	XP_011518179.1:n.-161-5292C>G
XM_017017167.1:c.-499-4235C>G (LRRC56)	XP_016872656.1:n.-499-4235C>G
XM_017017168.1:c.-499-4235C>G (LRRC56)	XP_016872657.1:n.-499-4235C>G
NM_005343.4:c.35G>C (HRAS) MANE Select	NP_005334.1:p.Gly12Ala
NM_001318054.2:c.-285G>C (HRAS)	NP_001304983.1:n.-285G>C
NM_001130442.3:c.35G>C (HRAS)	NP_001123914.1:p.Gly12Ala
NM_176795.5:c.35G>C (HRAS) MANE Plus Clinical	NP_789765.1:p.Gly12Ala