Canonical Allele Identifier: CA1947153570
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.533976_533989delinsAGGACCTTCCGTGG , CM000673.2:g.533976_533989delinsAGGACCTTCCGTGG GRCh38
NC_000011.9:g.533976_533989delinsAGGACCTTCCGTGG , CM000673.1:g.533976_533989delinsAGGACCTTCCGTGG GRCh37
NC_000011.8:g.523976_523989delinsAGGACCTTCCGTGG NCBI36
NG_007666.1:g.6562_6575delinsCCACGGAAGGTCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.112-45_112-32delinsCCACGGAAGGTCCT (HRAS) ENSP00000380722.3:n.112-45_112-32delinsCCACGGAAGGTCCT
ENST00000417302.7:c.112-45_112-32delinsCCACGGAAGGTCCT (HRAS) MANE Plus Clinical ENSP00000388246.1:n.112-45_112-32delinsCCACGGAAGGTCCT
ENST00000417302.6:c.112-45_112-32delinsCCACGGAAGGTCCT (HRAS) ENSP00000388246.1:n.112-45_112-32delinsCCACGGAAGGTCCT
ENST00000462734.2:c.112-45_112-32delinsCCACGGAAGGTCCT (HRAS) ENSP00000507303.1:n.112-45_112-32delinsCCACGGAAGGTCCT
ENST00000311189.8:c.112-45_112-32delinsCCACGGAAGGTCCT (HRAS) MANE Select ENSP00000309845.7:n.112-45_112-32delinsCCACGGAAGGTCCT
ENST00000311189.7:c.112-45_112-32delinsCCACGGAAGGTCCT (HRAS) ENSP00000309845.7:n.112-45_112-32delinsCCACGGAAGGTCCT
ENST00000397594.5:c.112-45_112-32delinsCCACGGAAGGTCCT (HRAS) ENSP00000380722.1:n.112-45_112-32delinsCCACGGAAGGTCCT
ENST00000397596.6:c.112-45_112-32delinsCCACGGAAGGTCCT (HRAS) ENSP00000380723.2:n.112-45_112-32delinsCCACGGAAGGTCCT
ENST00000417302.5:c.112-45_112-32delinsCCACGGAAGGTCCT (HRAS) ENSP00000388246.1:n.112-45_112-32delinsCCACGGAAGGTCCT
ENST00000451590.5:c.112-45_112-32delinsCCACGGAAGGTCCT (HRAS) ENSP00000407586.1:n.112-45_112-32delinsCCACGGAAGGTCCT
ENST00000468682.2:n.600-45_600-32delinsCCACGGAAGGTCCT (HRAS)
ENST00000493230.5:c.112-45_112-32delinsCCACGGAAGGTCCT (HRAS) ENSP00000434023.1:n.112-45_112-32delinsCCACGGAAGGTCCT
NM_001130442.1:c.112-45_112-32delinsCCACGGAAGGTCCT (HRAS) NP_001123914.1:n.112-45_112-32delinsCCACGGAAGGTCCT
NM_005343.2:c.112-45_112-32delinsCCACGGAAGGTCCT (HRAS) NP_005334.1:n.112-45_112-32delinsCCACGGAAGGTCCT
NM_176795.3:c.112-45_112-32delinsCCACGGAAGGTCCT (HRAS) NP_789765.1:n.112-45_112-32delinsCCACGGAAGGTCCT
XM_011519875.1:c.-424-4622_-424-4609delinsAGGACCTTCCGTGG (LRRC56) XP_011518177.1:n.-424-4622_-424-4609delinsAGGACCTTCCGTGG
XM_011519877.1:c.-161-5604_-161-5591delinsAGGACCTTCCGTGG (LRRC56) XP_011518179.1:n.-161-5604_-161-5591delinsAGGACCTTCCGTGG
XR_242795.1:n.311-45_311-32delinsCCACGGAAGGTCCT (HRAS)
NM_001130442.2:c.112-45_112-32delinsCCACGGAAGGTCCT (HRAS) NP_001123914.1:n.112-45_112-32delinsCCACGGAAGGTCCT
NM_001318054.1:c.-208-45_-208-32delinsCCACGGAAGGTCCT (HRAS) NP_001304983.1:n.-208-45_-208-32delinsCCACGGAAGGTCCT
NM_005343.3:c.112-45_112-32delinsCCACGGAAGGTCCT (HRAS) NP_005334.1:n.112-45_112-32delinsCCACGGAAGGTCCT
NM_176795.4:c.112-45_112-32delinsCCACGGAAGGTCCT (HRAS) NP_789765.1:n.112-45_112-32delinsCCACGGAAGGTCCT
XM_011519875.2:c.-424-4622_-424-4609delinsAGGACCTTCCGTGG (LRRC56) XP_011518177.1:n.-424-4622_-424-4609delinsAGGACCTTCCGTGG
XM_011519877.2:c.-161-5604_-161-5591delinsAGGACCTTCCGTGG (LRRC56) XP_011518179.1:n.-161-5604_-161-5591delinsAGGACCTTCCGTGG
XM_017017167.1:c.-499-4547_-499-4534delinsAGGACCTTCCGTGG (LRRC56) XP_016872656.1:n.-499-4547_-499-4534delinsAGGACCTTCCGTGG
XM_017017168.1:c.-499-4547_-499-4534delinsAGGACCTTCCGTGG (LRRC56) XP_016872657.1:n.-499-4547_-499-4534delinsAGGACCTTCCGTGG
NM_005343.4:c.112-45_112-32delinsCCACGGAAGGTCCT (HRAS) MANE Select NP_005334.1:n.112-45_112-32delinsCCACGGAAGGTCCT
NM_001318054.2:c.-208-45_-208-32delinsCCACGGAAGGTCCT (HRAS) NP_001304983.1:n.-208-45_-208-32delinsCCACGGAAGGTCCT
NM_001130442.3:c.112-45_112-32delinsCCACGGAAGGTCCT (HRAS) NP_001123914.1:n.112-45_112-32delinsCCACGGAAGGTCCT
NM_176795.5:c.112-45_112-32delinsCCACGGAAGGTCCT (HRAS) MANE Plus Clinical NP_789765.1:n.112-45_112-32delinsCCACGGAAGGTCCT
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