Canonical Allele Identifier: CA2580083848
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

ClinVar Variation Id: 1711126
ClinVar RCV Id: RCV002292420
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.533910del , CM000673.2:g.533910del GRCh38
NC_000011.9:g.533910del , CM000673.1:g.533910del GRCh37
NC_000011.8:g.523910del NCBI36
NG_007666.1:g.6641del

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.146del (HRAS) ENSP00000380722.3:p.Glu49GlyfsTer?
ENST00000417302.7:c.146del (HRAS) MANE Plus Clinical ENSP00000388246.1:p.Glu49GlyfsTer?
ENST00000417302.6:c.146del (HRAS) ENSP00000388246.1:p.Glu49GlyfsTer?
ENST00000462734.2:c.146del (HRAS) ENSP00000507303.1:p.Glu49GlyfsTer?
ENST00000311189.8:c.146del (HRAS) MANE Select ENSP00000309845.7:p.Glu49GlyfsTer?
ENST00000311189.7:c.146del (HRAS) ENSP00000309845.7:p.Glu49GlyfsTer?
ENST00000397594.5:c.146del (HRAS) ENSP00000380722.1:p.Glu49GlyfsTer?
ENST00000397596.6:c.146del (HRAS) ENSP00000380723.2:p.Glu49GlyfsTer?
ENST00000417302.5:c.146del (HRAS) ENSP00000388246.1:p.Glu49GlyfsTer?
ENST00000451590.5:c.146del (HRAS) ENSP00000407586.1:p.Glu49GlyfsTer?
ENST00000468682.2:n.634del (HRAS)
ENST00000479482.1:n.67del (HRAS)
ENST00000493230.5:c.146del (HRAS) ENSP00000434023.1:p.Glu49GlyfsTer?
NM_001130442.1:c.146del (HRAS) NP_001123914.1:p.Glu49GlyfsTer?
NM_005343.2:c.146del (HRAS) NP_005334.1:p.Glu49GlyfsTer?
NM_176795.3:c.146del (HRAS) NP_789765.1:p.Glu49GlyfsTer?
XM_011519875.1:c.-424-4688del (LRRC56) XP_011518177.1:n.-424-4688del
XM_011519877.1:c.-162+5573del (LRRC56) XP_011518179.1:n.-162+5573del
XR_242795.1:n.345del (HRAS)
NM_001130442.2:c.146del (HRAS) NP_001123914.1:p.Glu49GlyfsTer?
NM_001318054.1:c.-174del (HRAS) NP_001304983.1:n.-174del
NM_005343.3:c.146del (HRAS) NP_005334.1:p.Glu49GlyfsTer?
NM_176795.4:c.146del (HRAS) NP_789765.1:p.Glu49GlyfsTer?
XM_011519875.2:c.-424-4688del (LRRC56) XP_011518177.1:n.-424-4688del
XM_011519877.2:c.-162+5573del (LRRC56) XP_011518179.1:n.-162+5573del
XM_017017167.1:c.-499-4613del (LRRC56) XP_016872656.1:n.-499-4613del
XM_017017168.1:c.-499-4613del (LRRC56) XP_016872657.1:n.-499-4613del
NM_005343.4:c.146del (HRAS) MANE Select NP_005334.1:p.Glu49GlyfsTer?
NM_001318054.2:c.-174del (HRAS) NP_001304983.1:n.-174del
NM_001130442.3:c.146del (HRAS) NP_001123914.1:p.Glu49GlyfsTer?
NM_176795.5:c.146del (HRAS) MANE Plus Clinical NP_789765.1:p.Glu49GlyfsTer?
Search 100 bp 5'
Search 100 bp 3'