Canonical Allele Identifier: CA1947140525
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532439_532447delinsCCTTCCTTG , CM000673.2:g.532439_532447delinsCCTTCCTTG GRCh38
NC_000011.9:g.532439_532447delinsCCTTCCTTG , CM000673.1:g.532439_532447delinsCCTTCCTTG GRCh37
NC_000011.8:g.522439_522447delinsCCTTCCTTG NCBI36
NG_007666.1:g.8104_8112delinsCAAGGAAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*203_*211delinsCAAGGAAGG (HRAS) ENSP00000380722.3:n.*203_*211delinsCAAGGAAGG
ENST00000417302.7:c.*328_*336delinsCAAGGAAGG (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*328_*336delinsCAAGGAAGG
ENST00000397594.6:c.434_442delinsCAAGGAAGG (HRAS) ENSP00000380722.2:n.434_442delinsCAAGGAAGG
ENST00000417302.6:c.*328_*336delinsCAAGGAAGG (HRAS) ENSP00000388246.1:n.*328_*336delinsCAAGGAAGG
ENST00000462734.2:c.*263_*271delinsCAAGGAAGG (HRAS) ENSP00000507303.1:n.*263_*271delinsCAAGGAAGG
ENST00000311189.8:c.*81_*89delinsCAAGGAAGG (HRAS) MANE Select ENSP00000309845.7:n.*81_*89delinsCAAGGAAGG
ENST00000311189.7:c.*81_*89delinsCAAGGAAGG (HRAS) ENSP00000309845.7:n.*81_*89delinsCAAGGAAGG
ENST00000397594.5:c.*328_*336delinsCAAGGAAGG (HRAS) ENSP00000380722.1:n.*328_*336delinsCAAGGAAGG
ENST00000397596.6:c.*189_*197delinsCAAGGAAGG (HRAS) ENSP00000380723.2:n.*189_*197delinsCAAGGAAGG
ENST00000417302.5:c.*328_*336delinsCAAGGAAGG (HRAS) ENSP00000388246.1:n.*328_*336delinsCAAGGAAGG
ENST00000451590.5:c.*189_*197delinsCAAGGAAGG (HRAS) ENSP00000407586.1:n.*189_*197delinsCAAGGAAGG
ENST00000462734.1:n.426_434delinsCAAGGAAGG (HRAS)
ENST00000478324.5:n.426_434delinsCAAGGAAGG (HRAS)
ENST00000493230.5:c.*220_*228delinsCAAGGAAGG (HRAS) ENSP00000434023.1:n.*220_*228delinsCAAGGAAGG
NM_001130442.1:c.*189_*197delinsCAAGGAAGG (HRAS) NP_001123914.1:n.*189_*197delinsCAAGGAAGG
NM_005343.2:c.*81_*89delinsCAAGGAAGG (HRAS) NP_005334.1:n.*81_*89delinsCAAGGAAGG
NM_176795.3:c.*328_*336delinsCAAGGAAGG (HRAS) NP_789765.1:n.*328_*336delinsCAAGGAAGG
XM_011519875.1:c.-425+4102_-425+4110delinsCCTTCCTTG (LRRC56) XP_011518177.1:n.-425+4102_-425+4110delinsCCTTCCTTG
XM_011519877.1:c.-162+4102_-162+4110delinsCCTTCCTTG (LRRC56) XP_011518179.1:n.-162+4102_-162+4110delinsCCTTCCTTG
XR_242795.1:n.932_940delinsCAAGGAAGG (HRAS)
NM_001130442.2:c.*189_*197delinsCAAGGAAGG (HRAS) NP_001123914.1:n.*189_*197delinsCAAGGAAGG
NM_001318054.1:c.*81_*89delinsCAAGGAAGG (HRAS) NP_001304983.1:n.*81_*89delinsCAAGGAAGG
NM_005343.3:c.*81_*89delinsCAAGGAAGG (HRAS) NP_005334.1:n.*81_*89delinsCAAGGAAGG
NM_176795.4:c.*328_*336delinsCAAGGAAGG (HRAS) NP_789765.1:n.*328_*336delinsCAAGGAAGG
XM_011519875.2:c.-425+4102_-425+4110delinsCCTTCCTTG (LRRC56) XP_011518177.1:n.-425+4102_-425+4110delinsCCTTCCTTG
XM_011519877.2:c.-162+4102_-162+4110delinsCCTTCCTTG (LRRC56) XP_011518179.1:n.-162+4102_-162+4110delinsCCTTCCTTG
XM_017017167.1:c.-500+4102_-500+4110delinsCCTTCCTTG (LRRC56) XP_016872656.1:n.-500+4102_-500+4110delinsCCTTCCTTG
XM_017017168.1:c.-500+4102_-500+4110delinsCCTTCCTTG (LRRC56) XP_016872657.1:n.-500+4102_-500+4110delinsCCTTCCTTG
NM_005343.4:c.*81_*89delinsCAAGGAAGG (HRAS) MANE Select NP_005334.1:n.*81_*89delinsCAAGGAAGG
NM_001318054.2:c.*81_*89delinsCAAGGAAGG (HRAS) NP_001304983.1:n.*81_*89delinsCAAGGAAGG
NM_001130442.3:c.*189_*197delinsCAAGGAAGG (HRAS) NP_001123914.1:n.*189_*197delinsCAAGGAAGG
NM_176795.5:c.*328_*336delinsCAAGGAAGG (HRAS) MANE Plus Clinical NP_789765.1:n.*328_*336delinsCAAGGAAGG
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