Canonical Allele Identifier: CA1139661725

Gene: HRAS LRRC56

Linked Data

• ClinVar Variation Id: 951790
• ClinVar RCV Id: RCV001223776
• dbSNP Id: rs1851237302

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.533474_533493del , CM000673.2:g.533474_533493del	GRCh38
NC_000011.9:g.533474_533493del , CM000673.1:g.533474_533493del	GRCh37
NC_000011.8:g.523474_523493del	NCBI36
NG_007666.1:g.7060_7079del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397594.7:c.412_431del (HRAS)	ENSP00000380722.3:p.Gly138LeufsTer13
ENST00000417302.7:c.412_431del (HRAS) MANE Plus Clinical	ENSP00000388246.1:p.Gly138LeufsTer13
ENST00000397594.6:c.130_149del (HRAS)	ENSP00000380722.2:p.Gly44LeufsTer13
ENST00000417302.6:c.412_431del (HRAS)	ENSP00000388246.1:p.Gly138LeufsTer13
ENST00000462734.2:c.412_431del (HRAS)	ENSP00000507303.1:p.Gly138LeufsTer?
ENST00000311189.8:c.412_431del (HRAS) MANE Select	ENSP00000309845.7:p.Gly138LeufsTer18
ENST00000311189.7:c.412_431del (HRAS)	ENSP00000309845.7:p.Gly138LeufsTer18
ENST00000397594.5:c.412_431del (HRAS)	ENSP00000380722.1:p.Gly138LeufsTer13
ENST00000397596.6:c.412_431del (HRAS)	ENSP00000380723.2:p.Gly138LeufsTer18
ENST00000417302.5:c.412_431del (HRAS)	ENSP00000388246.1:p.Gly138LeufsTer13
ENST00000451590.5:c.412_431del (HRAS)	ENSP00000407586.1:p.Gly138LeufsTer18
ENST00000462734.1:n.105_124del (HRAS)
ENST00000478324.5:n.122_141del (HRAS)
ENST00000479482.1:n.333_352del (HRAS)
ENST00000493230.5:c.412_431del (HRAS)	ENSP00000434023.1:p.Gly138LeufsTer13
NM_001130442.1:c.412_431del (HRAS)	NP_001123914.1:p.Gly138LeufsTer18
NM_005343.2:c.412_431del (HRAS)	NP_005334.1:p.Gly138LeufsTer18
NM_176795.3:c.412_431del (HRAS)	NP_789765.1:p.Gly138LeufsTer13
XM_011519875.1:c.-424-5124_-424-5105del (LRRC56)	XP_011518177.1:n.-424-5124_-424-5105del
XM_011519877.1:c.-162+5137_-162+5156del (LRRC56)	XP_011518179.1:n.-162+5137_-162+5156del
XR_242795.1:n.611_630del (HRAS)
NM_001130442.2:c.412_431del (HRAS)	NP_001123914.1:p.Gly138LeufsTer18
NM_001318054.1:c.93_112del (HRAS)	NP_001304983.1:p.Ala32SerfsTer27
NM_005343.3:c.412_431del (HRAS)	NP_005334.1:p.Gly138LeufsTer18
NM_176795.4:c.412_431del (HRAS)	NP_789765.1:p.Gly138LeufsTer13
XM_011519875.2:c.-424-5124_-424-5105del (LRRC56)	XP_011518177.1:n.-424-5124_-424-5105del
XM_011519877.2:c.-162+5137_-162+5156del (LRRC56)	XP_011518179.1:n.-162+5137_-162+5156del
XM_017017167.1:c.-499-5049_-499-5030del (LRRC56)	XP_016872656.1:n.-499-5049_-499-5030del
XM_017017168.1:c.-499-5049_-499-5030del (LRRC56)	XP_016872657.1:n.-499-5049_-499-5030del
NM_005343.4:c.412_431del (HRAS) MANE Select	NP_005334.1:p.Gly138LeufsTer18
NM_001318054.2:c.93_112del (HRAS)	NP_001304983.1:p.Ala32SerfsTer27
NM_001130442.3:c.412_431del (HRAS)	NP_001123914.1:p.Gly138LeufsTer18
NM_176795.5:c.412_431del (HRAS) MANE Plus Clinical	NP_789765.1:p.Gly138LeufsTer13