Canonical Allele Identifier: CA183175

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 178860
• ClinVar RCV Id: RCV000155632 ; RCV000694918 ; RCV002514997
• dbSNP Id: rs727504496
• ExAC: 11:534292 C / T
• gnomAD v2: 11-534292-C-T
• gnomAD v3: 11-534292-C-T
• gnomAD v4: 11-534292-C-T
• MyVariant Identifiers: chr11:g.534292C>T (hg19) ; chr11:g.534292C>T (hg38)
• PubMed: PMID:8605880 ; PMID:22683711 ; PMID:24259709

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.534292C>T , CM000673.2:g.534292C>T	GRCh38
NC_000011.9:g.534292C>T , CM000673.1:g.534292C>T	GRCh37
NC_000011.8:g.524292C>T	NCBI36
NG_007666.1:g.6259G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000397594.7:c.31G>A (HRAS)	ENSP00000380722.3:p.Ala11Thr
ENST00000417302.7:c.31G>A (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Ala11Thr
ENST00000417302.6:c.31G>A (HRAS)	ENSP00000388246.1:p.Ala11Thr
ENST00000462734.2:c.31G>A (HRAS)	ENSP00000507303.1:p.Ala11Thr
ENST00000311189.8:c.31G>A (HRAS) MANE Select	ENSP00000309845.7:p.Ala11Thr
ENST00000311189.7:c.31G>A (HRAS)	ENSP00000309845.7:p.Ala11Thr
ENST00000397594.5:c.31G>A (HRAS)	ENSP00000380722.1:p.Ala11Thr
ENST00000397596.6:c.31G>A (HRAS)	ENSP00000380723.2:p.Ala11Thr
ENST00000417302.5:c.31G>A (HRAS)	ENSP00000388246.1:p.Ala11Thr
ENST00000451590.5:c.31G>A (HRAS)	ENSP00000407586.1:p.Ala11Thr
ENST00000468682.2:n.519G>A (HRAS)
ENST00000482021.1:n.154G>A (HRAS)
ENST00000493230.5:c.31G>A (HRAS)	ENSP00000434023.1:p.Ala11Thr
NM_001130442.1:c.31G>A (HRAS)	NP_001123914.1:p.Ala11Thr
NM_005343.2:c.31G>A (HRAS)	NP_005334.1:p.Ala11Thr
NM_176795.3:c.31G>A (HRAS)	NP_789765.1:p.Ala11Thr
XM_011519875.1:c.-424-4306C>T (LRRC56)	XP_011518177.1:n.-424-4306C>T
XM_011519877.1:c.-161-5288C>T (LRRC56)	XP_011518179.1:n.-161-5288C>T
XR_242795.1:n.230G>A (HRAS)
NM_001130442.2:c.31G>A (HRAS)	NP_001123914.1:p.Ala11Thr
NM_001318054.1:c.-289G>A (HRAS)	NP_001304983.1:n.-289G>A
NM_005343.3:c.31G>A (HRAS)	NP_005334.1:p.Ala11Thr
NM_176795.4:c.31G>A (HRAS)	NP_789765.1:p.Ala11Thr
XM_011519875.2:c.-424-4306C>T (LRRC56)	XP_011518177.1:n.-424-4306C>T
XM_011519877.2:c.-161-5288C>T (LRRC56)	XP_011518179.1:n.-161-5288C>T
XM_017017167.1:c.-499-4231C>T (LRRC56)	XP_016872656.1:n.-499-4231C>T
XM_017017168.1:c.-499-4231C>T (LRRC56)	XP_016872657.1:n.-499-4231C>T
NM_005343.4:c.31G>A (HRAS) MANE Select	NP_005334.1:p.Ala11Thr
NM_001318054.2:c.-289G>A (HRAS)	NP_001304983.1:n.-289G>A
NM_001130442.3:c.31G>A (HRAS)	NP_001123914.1:p.Ala11Thr
NM_176795.5:c.31G>A (HRAS) MANE Plus Clinical	NP_789765.1:p.Ala11Thr