Canonical Allele Identifier: CA1139661722
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

ClinVar Variation Id: 976046
ClinVar RCV Id: RCV001253224
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532574_534004del , CM000673.2:g.532574_534004del GRCh38
NC_000011.9:g.532574_534004del , CM000673.1:g.532574_534004del GRCh37
NC_000011.8:g.522574_524004del NCBI36
NG_007666.1:g.6548_7978del

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.112-59_*77del (HRAS)
ENST00000417302.7:c.112-59_*202del (HRAS)
ENST00000417302.6:c.112-59_*202del (HRAS)
ENST00000462734.2:c.112-59_*188-51del (HRAS)
ENST00000311189.8:c.112-59_*6-51del (HRAS)
ENST00000311189.7:c.112-59_*6-51del (HRAS)
ENST00000397594.5:c.112-59_*202del (HRAS)
ENST00000397596.6:c.112-59_*63del (HRAS)
ENST00000417302.5:c.112-59_*202del (HRAS)
ENST00000451590.5:c.112-59_*63del (HRAS)
ENST00000493230.5:c.112-59_*145-51del (HRAS)
NM_001130442.1:c.112-59_*63del (HRAS)
NM_005343.2:c.112-59_*6-51del (HRAS)
NM_176795.3:c.112-59_*202del (HRAS)
XM_011519875.1:c.-425+4237_-424-4594del (LRRC56) XP_011518177.1:n.-425+4237_-424-4594del
XM_011519877.1:c.-162+4237_-161-5576del (LRRC56) XP_011518179.1:n.-162+4237_-161-5576del
XR_242795.1:n.311-59_857-51del (HRAS)
NM_001130442.2:c.112-59_*63del (HRAS)
NM_001318054.1:c.-208-59_*6-51del (HRAS)
NM_005343.3:c.112-59_*6-51del (HRAS)
NM_176795.4:c.112-59_*202del (HRAS)
XM_011519875.2:c.-425+4237_-424-4594del (LRRC56) XP_011518177.1:n.-425+4237_-424-4594del
XM_011519877.2:c.-162+4237_-161-5576del (LRRC56) XP_011518179.1:n.-162+4237_-161-5576del
XM_017017167.1:c.-500+4237_-499-4519del (LRRC56) XP_016872656.1:n.-500+4237_-499-4519del
XM_017017168.1:c.-500+4237_-499-4519del (LRRC56) XP_016872657.1:n.-500+4237_-499-4519del
NM_005343.4:c.112-59_*6-51del (HRAS)
NM_001318054.2:c.-208-59_*6-51del (HRAS)
NM_001130442.3:c.112-59_*63del (HRAS)
NM_176795.5:c.112-59_*202del (HRAS)
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