Canonical Allele Identifier: CA1947140519
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532437_532453delinsTTCCTTCCTTGCTTCCG , CM000673.2:g.532437_532453delinsTTCCTTCCTTGCTTCCG GRCh38
NC_000011.9:g.532437_532453delinsTTCCTTCCTTGCTTCCG , CM000673.1:g.532437_532453delinsTTCCTTCCTTGCTTCCG GRCh37
NC_000011.8:g.522437_522453delinsTTCCTTCCTTGCTTCCG NCBI36
NG_007666.1:g.8098_8114delinsCGGAAGCAAGGAAGGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*197_*213delinsCGGAAGCAAGGAAGGAA (HRAS) ENSP00000380722.3:n.*197_*213delinsCGGAAGCAAGGAAGGAA
ENST00000417302.7:c.*322_*338delinsCGGAAGCAAGGAAGGAA (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*322_*338delinsCGGAAGCAAGGAAGGAA
ENST00000397594.6:c.428_444delinsCGGAAGCAAGGAAGGAA (HRAS) ENSP00000380722.2:n.428_444delinsCGGAAGCAAGGAAGGAA
ENST00000417302.6:c.*322_*338delinsCGGAAGCAAGGAAGGAA (HRAS) ENSP00000388246.1:n.*322_*338delinsCGGAAGCAAGGAAGGAA
ENST00000462734.2:c.*257_*273delinsCGGAAGCAAGGAAGGAA (HRAS) ENSP00000507303.1:n.*257_*273delinsCGGAAGCAAGGAAGGAA
ENST00000311189.8:c.*75_*91delinsCGGAAGCAAGGAAGGAA (HRAS) MANE Select ENSP00000309845.7:n.*75_*91delinsCGGAAGCAAGGAAGGAA
ENST00000311189.7:c.*75_*91delinsCGGAAGCAAGGAAGGAA (HRAS) ENSP00000309845.7:n.*75_*91delinsCGGAAGCAAGGAAGGAA
ENST00000397594.5:c.*322_*338delinsCGGAAGCAAGGAAGGAA (HRAS) ENSP00000380722.1:n.*322_*338delinsCGGAAGCAAGGAAGGAA
ENST00000397596.6:c.*183_*199delinsCGGAAGCAAGGAAGGAA (HRAS) ENSP00000380723.2:n.*183_*199delinsCGGAAGCAAGGAAGGAA
ENST00000417302.5:c.*322_*338delinsCGGAAGCAAGGAAGGAA (HRAS) ENSP00000388246.1:n.*322_*338delinsCGGAAGCAAGGAAGGAA
ENST00000451590.5:c.*183_*199delinsCGGAAGCAAGGAAGGAA (HRAS) ENSP00000407586.1:n.*183_*199delinsCGGAAGCAAGGAAGGAA
ENST00000462734.1:n.420_436delinsCGGAAGCAAGGAAGGAA (HRAS)
ENST00000478324.5:n.420_436delinsCGGAAGCAAGGAAGGAA (HRAS)
ENST00000493230.5:c.*214_*230delinsCGGAAGCAAGGAAGGAA (HRAS) ENSP00000434023.1:n.*214_*230delinsCGGAAGCAAGGAAGGAA
NM_001130442.1:c.*183_*199delinsCGGAAGCAAGGAAGGAA (HRAS) NP_001123914.1:n.*183_*199delinsCGGAAGCAAGGAAGGAA
NM_005343.2:c.*75_*91delinsCGGAAGCAAGGAAGGAA (HRAS) NP_005334.1:n.*75_*91delinsCGGAAGCAAGGAAGGAA
NM_176795.3:c.*322_*338delinsCGGAAGCAAGGAAGGAA (HRAS) NP_789765.1:n.*322_*338delinsCGGAAGCAAGGAAGGAA
XM_011519875.1:c.-425+4100_-425+4116delinsTTCCTTCCTTGCTTCCG (LRRC56) XP_011518177.1:n.-425+4100_-425+4116delinsTTCCTTCCTTGCTTCCG
XM_011519877.1:c.-162+4100_-162+4116delinsTTCCTTCCTTGCTTCCG (LRRC56) XP_011518179.1:n.-162+4100_-162+4116delinsTTCCTTCCTTGCTTCCG
XR_242795.1:n.926_942delinsCGGAAGCAAGGAAGGAA (HRAS)
NM_001130442.2:c.*183_*199delinsCGGAAGCAAGGAAGGAA (HRAS) NP_001123914.1:n.*183_*199delinsCGGAAGCAAGGAAGGAA
NM_001318054.1:c.*75_*91delinsCGGAAGCAAGGAAGGAA (HRAS) NP_001304983.1:n.*75_*91delinsCGGAAGCAAGGAAGGAA
NM_005343.3:c.*75_*91delinsCGGAAGCAAGGAAGGAA (HRAS) NP_005334.1:n.*75_*91delinsCGGAAGCAAGGAAGGAA
NM_176795.4:c.*322_*338delinsCGGAAGCAAGGAAGGAA (HRAS) NP_789765.1:n.*322_*338delinsCGGAAGCAAGGAAGGAA
XM_011519875.2:c.-425+4100_-425+4116delinsTTCCTTCCTTGCTTCCG (LRRC56) XP_011518177.1:n.-425+4100_-425+4116delinsTTCCTTCCTTGCTTCCG
XM_011519877.2:c.-162+4100_-162+4116delinsTTCCTTCCTTGCTTCCG (LRRC56) XP_011518179.1:n.-162+4100_-162+4116delinsTTCCTTCCTTGCTTCCG
XM_017017167.1:c.-500+4100_-500+4116delinsTTCCTTCCTTGCTTCCG (LRRC56) XP_016872656.1:n.-500+4100_-500+4116delinsTTCCTTCCTTGCTTCCG
XM_017017168.1:c.-500+4100_-500+4116delinsTTCCTTCCTTGCTTCCG (LRRC56) XP_016872657.1:n.-500+4100_-500+4116delinsTTCCTTCCTTGCTTCCG
NM_005343.4:c.*75_*91delinsCGGAAGCAAGGAAGGAA (HRAS) MANE Select NP_005334.1:n.*75_*91delinsCGGAAGCAAGGAAGGAA
NM_001318054.2:c.*75_*91delinsCGGAAGCAAGGAAGGAA (HRAS) NP_001304983.1:n.*75_*91delinsCGGAAGCAAGGAAGGAA
NM_001130442.3:c.*183_*199delinsCGGAAGCAAGGAAGGAA (HRAS) NP_001123914.1:n.*183_*199delinsCGGAAGCAAGGAAGGAA
NM_176795.5:c.*322_*338delinsCGGAAGCAAGGAAGGAA (HRAS) MANE Plus Clinical NP_789765.1:n.*322_*338delinsCGGAAGCAAGGAAGGAA
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