Canonical Allele Identifier: CA2697558804

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 2737254
• ClinVar RCV Id: RCV003516394

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.533478_533480del , CM000673.2:g.533478_533480del	GRCh38
NC_000011.9:g.533478_533480del , CM000673.1:g.533478_533480del	GRCh37
NC_000011.8:g.523478_523480del	NCBI36
NG_007666.1:g.7072_7074del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.424_426del (HRAS)	ENSP00000380722.3:p.Ile142del
ENST00000417302.7:c.424_426del (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Ile142del
ENST00000397594.6:c.142_144del (HRAS)	ENSP00000380722.2:p.Ile48del
ENST00000417302.6:c.424_426del (HRAS)	ENSP00000388246.1:p.Ile142del
ENST00000462734.2:c.424_426del (HRAS)	ENSP00000507303.1:p.Ile142del
ENST00000311189.8:c.424_426del (HRAS) MANE Select	ENSP00000309845.7:p.Ile142del
ENST00000311189.7:c.424_426del (HRAS)	ENSP00000309845.7:p.Ile142del
ENST00000397594.5:c.424_426del (HRAS)	ENSP00000380722.1:p.Ile142del
ENST00000397596.6:c.424_426del (HRAS)	ENSP00000380723.2:p.Ile142del
ENST00000417302.5:c.424_426del (HRAS)	ENSP00000388246.1:p.Ile142del
ENST00000451590.5:c.424_426del (HRAS)	ENSP00000407586.1:p.Ile142del
ENST00000462734.1:n.117_119del (HRAS)
ENST00000478324.5:n.134_136del (HRAS)
ENST00000479482.1:n.345_347del (HRAS)
ENST00000493230.5:c.424_426del (HRAS)	ENSP00000434023.1:p.Ile142del
NM_001130442.1:c.424_426del (HRAS)	NP_001123914.1:p.Ile142del
NM_005343.2:c.424_426del (HRAS)	NP_005334.1:p.Ile142del
NM_176795.3:c.424_426del (HRAS)	NP_789765.1:p.Ile142del
XM_011519875.1:c.-424-5120_-424-5118del (LRRC56)	XP_011518177.1:n.-424-5120_-424-5118del
XM_011519877.1:c.-162+5141_-162+5143del (LRRC56)	XP_011518179.1:n.-162+5141_-162+5143del
XR_242795.1:n.623_625del (HRAS)
NM_001130442.2:c.424_426del (HRAS)	NP_001123914.1:p.Ile142del
NM_001318054.1:c.105_107del (HRAS)	NP_001304983.1:p.Ser36del
NM_005343.3:c.424_426del (HRAS)	NP_005334.1:p.Ile142del
NM_176795.4:c.424_426del (HRAS)	NP_789765.1:p.Ile142del
XM_011519875.2:c.-424-5120_-424-5118del (LRRC56)	XP_011518177.1:n.-424-5120_-424-5118del
XM_011519877.2:c.-162+5141_-162+5143del (LRRC56)	XP_011518179.1:n.-162+5141_-162+5143del
XM_017017167.1:c.-499-5045_-499-5043del (LRRC56)	XP_016872656.1:n.-499-5045_-499-5043del
XM_017017168.1:c.-499-5045_-499-5043del (LRRC56)	XP_016872657.1:n.-499-5045_-499-5043del
NM_005343.4:c.424_426del (HRAS) MANE Select	NP_005334.1:p.Ile142del
NM_001318054.2:c.105_107del (HRAS)	NP_001304983.1:p.Ser36del
NM_001130442.3:c.424_426del (HRAS)	NP_001123914.1:p.Ile142del
NM_176795.5:c.424_426del (HRAS) MANE Plus Clinical	NP_789765.1:p.Ile142del