Canonical Allele Identifier: CA295247

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 12606
• ClinVar RCV Id: RCV000013440 ; RCV000149831 ; RCV000207504 ; RCV000417661 ; RCV000420958 ; RCV000423190 ; RCV000424247 ; RCV000425964 ; RCV000426653 ; RCV000428812 ; RCV000431688 ; RCV000433893 ; RCV000434069 ; RCV000436007 ; RCV000436205 ; RCV000439052 ; RCV000439954 ; RCV000441514 ; RCV000444110 ; RCV000445225 ; RCV000445336 ; RCV000678903 ; RCV000762847 ; RCV001813188
• dbSNP Id: rs104894228
• COSMIC: COSM488 ; COSM689078
• MyVariant Identifiers: chr11:g.534286C>A (hg19) ; chr11:g.534286C>A (hg38)
• ERepo: CA295247/MONDO:0018997/004
• PubMed: PMID:16329078 ; PMID:16372351 ; PMID:16835863 ; PMID:17211612 ; PMID:17384584 ; PMID:19213030 ; PMID:19255327 ; PMID:19773371 ; PMID:21438134 ; PMID:21495179 ; PMID:23406027 ; PMID:25157968 ; PMID:26619011 ; PMID:168335863

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.534286C>A , CM000673.2:g.534286C>A	GRCh38
NC_000011.9:g.534286C>A , CM000673.1:g.534286C>A	GRCh37
NC_000011.8:g.524286C>A	NCBI36
NG_007666.1:g.6265G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000397594.7:c.37G>T (HRAS)	ENSP00000380722.3:p.Gly13Cys
ENST00000417302.7:c.37G>T (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Gly13Cys
ENST00000417302.6:c.37G>T (HRAS)	ENSP00000388246.1:p.Gly13Cys
ENST00000462734.2:c.37G>T (HRAS)	ENSP00000507303.1:p.Gly13Cys
ENST00000311189.8:c.37G>T (HRAS) MANE Select	ENSP00000309845.7:p.Gly13Cys
ENST00000311189.7:c.37G>T (HRAS)	ENSP00000309845.7:p.Gly13Cys
ENST00000397594.5:c.37G>T (HRAS)	ENSP00000380722.1:p.Gly13Cys
ENST00000397596.6:c.37G>T (HRAS)	ENSP00000380723.2:p.Gly13Cys
ENST00000417302.5:c.37G>T (HRAS)	ENSP00000388246.1:p.Gly13Cys
ENST00000451590.5:c.37G>T (HRAS)	ENSP00000407586.1:p.Gly13Cys
ENST00000468682.2:n.525G>T (HRAS)
ENST00000482021.1:n.160G>T (HRAS)
ENST00000493230.5:c.37G>T (HRAS)	ENSP00000434023.1:p.Gly13Cys
NM_001130442.1:c.37G>T (HRAS)	NP_001123914.1:p.Gly13Cys
NM_005343.2:c.37G>T (HRAS)	NP_005334.1:p.Gly13Cys
NM_176795.3:c.37G>T (HRAS)	NP_789765.1:p.Gly13Cys
XM_011519875.1:c.-424-4312C>A (LRRC56)	XP_011518177.1:n.-424-4312C>A
XM_011519877.1:c.-161-5294C>A (LRRC56)	XP_011518179.1:n.-161-5294C>A
XR_242795.1:n.236G>T (HRAS)
NM_001130442.2:c.37G>T (HRAS)	NP_001123914.1:p.Gly13Cys
NM_001318054.1:c.-283G>T (HRAS)	NP_001304983.1:n.-283G>T
NM_005343.3:c.37G>T (HRAS)	NP_005334.1:p.Gly13Cys
NM_176795.4:c.37G>T (HRAS)	NP_789765.1:p.Gly13Cys
XM_011519875.2:c.-424-4312C>A (LRRC56)	XP_011518177.1:n.-424-4312C>A
XM_011519877.2:c.-161-5294C>A (LRRC56)	XP_011518179.1:n.-161-5294C>A
XM_017017167.1:c.-499-4237C>A (LRRC56)	XP_016872656.1:n.-499-4237C>A
XM_017017168.1:c.-499-4237C>A (LRRC56)	XP_016872657.1:n.-499-4237C>A
NM_005343.4:c.37G>T (HRAS) MANE Select	NP_005334.1:p.Gly13Cys
NM_001318054.2:c.-283G>T (HRAS)	NP_001304983.1:n.-283G>T
NM_001130442.3:c.37G>T (HRAS)	NP_001123914.1:p.Gly13Cys
NM_176795.5:c.37G>T (HRAS) MANE Plus Clinical	NP_789765.1:p.Gly13Cys