Canonical Allele Identifier: CA2611691562
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

gnomAD v4: 11-532465-TCCTCCTTCCGTCTGCA-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532475_532490del , CM000673.2:g.532475_532490del GRCh38
NC_000011.9:g.532475_532490del , CM000673.1:g.532475_532490del GRCh37
NC_000011.8:g.522475_522490del NCBI36
NG_007666.1:g.8070_8085del

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*169_*184del (HRAS) ENSP00000380722.3:n.*169_*184del
ENST00000417302.7:c.*294_*309del (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*294_*309del
ENST00000397594.6:c.400_415del (HRAS) ENSP00000380722.2:n.400_415del
ENST00000417302.6:c.*294_*309del (HRAS) ENSP00000388246.1:n.*294_*309del
ENST00000462734.2:c.*229_*244del (HRAS) ENSP00000507303.1:n.*229_*244del
ENST00000311189.8:c.*47_*62del (HRAS) MANE Select ENSP00000309845.7:n.*47_*62del
ENST00000311189.7:c.*47_*62del (HRAS) ENSP00000309845.7:n.*47_*62del
ENST00000397594.5:c.*294_*309del (HRAS) ENSP00000380722.1:n.*294_*309del
ENST00000397596.6:c.*155_*170del (HRAS) ENSP00000380723.2:n.*155_*170del
ENST00000417302.5:c.*294_*309del (HRAS) ENSP00000388246.1:n.*294_*309del
ENST00000451590.5:c.*155_*170del (HRAS) ENSP00000407586.1:n.*155_*170del
ENST00000462734.1:n.392_407del (HRAS)
ENST00000478324.5:n.392_407del (HRAS)
ENST00000493230.5:c.*186_*201del (HRAS) ENSP00000434023.1:n.*186_*201del
NM_001130442.1:c.*155_*170del (HRAS) NP_001123914.1:n.*155_*170del
NM_005343.2:c.*47_*62del (HRAS) NP_005334.1:n.*47_*62del
NM_176795.3:c.*294_*309del (HRAS) NP_789765.1:n.*294_*309del
XM_011519875.1:c.-425+4138_-425+4153del (LRRC56) XP_011518177.1:n.-425+4138_-425+4153del
XM_011519877.1:c.-162+4138_-162+4153del (LRRC56) XP_011518179.1:n.-162+4138_-162+4153del
XR_242795.1:n.898_913del (HRAS)
NM_001130442.2:c.*155_*170del (HRAS) NP_001123914.1:n.*155_*170del
NM_001318054.1:c.*47_*62del (HRAS) NP_001304983.1:n.*47_*62del
NM_005343.3:c.*47_*62del (HRAS) NP_005334.1:n.*47_*62del
NM_176795.4:c.*294_*309del (HRAS) NP_789765.1:n.*294_*309del
XM_011519875.2:c.-425+4138_-425+4153del (LRRC56) XP_011518177.1:n.-425+4138_-425+4153del
XM_011519877.2:c.-162+4138_-162+4153del (LRRC56) XP_011518179.1:n.-162+4138_-162+4153del
XM_017017167.1:c.-500+4138_-500+4153del (LRRC56) XP_016872656.1:n.-500+4138_-500+4153del
XM_017017168.1:c.-500+4138_-500+4153del (LRRC56) XP_016872657.1:n.-500+4138_-500+4153del
NM_005343.4:c.*47_*62del (HRAS) MANE Select NP_005334.1:n.*47_*62del
NM_001318054.2:c.*47_*62del (HRAS) NP_001304983.1:n.*47_*62del
NM_001130442.3:c.*155_*170del (HRAS) NP_001123914.1:n.*155_*170del
NM_176795.5:c.*294_*309del (HRAS) MANE Plus Clinical NP_789765.1:n.*294_*309del
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