Canonical Allele Identifier: CA2611691027

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.533645_533670del , CM000673.2:g.533645_533670del GRCh38
NC_000011.9:g.533645_533670del , CM000673.1:g.533645_533670del GRCh37
NC_000011.8:g.523645_523670del NCBI36
NG_007666.1:g.6881_6906del

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.291-58_291-33del (HRAS) ENSP00000380722.3:n.291-58_291-33del
ENST00000417302.7:c.291-58_291-33del (HRAS) MANE Plus Clinical ENSP00000388246.1:n.291-58_291-33del
ENST00000397594.6:c.9-58_9-33del (HRAS) ENSP00000380722.2:n.9-58_9-33del
ENST00000417302.6:c.291-58_291-33del (HRAS) ENSP00000388246.1:n.291-58_291-33del
ENST00000462734.2:c.291-58_291-33del (HRAS) ENSP00000507303.1:n.291-58_291-33del
ENST00000311189.8:c.291-58_291-33del (HRAS) MANE Select ENSP00000309845.7:n.291-58_291-33del
ENST00000311189.7:c.291-58_291-33del (HRAS) ENSP00000309845.7:n.291-58_291-33del
ENST00000397594.5:c.291-58_291-33del (HRAS) ENSP00000380722.1:n.291-58_291-33del
ENST00000397596.6:c.291-58_291-33del (HRAS) ENSP00000380723.2:n.291-58_291-33del
ENST00000417302.5:c.291-58_291-33del (HRAS) ENSP00000388246.1:n.291-58_291-33del
ENST00000451590.5:c.291-58_291-33del (HRAS) ENSP00000407586.1:n.291-58_291-33del
ENST00000479482.1:n.212-58_212-33del (HRAS)
ENST00000493230.5:c.291-58_291-33del (HRAS) ENSP00000434023.1:n.291-58_291-33del
NM_001130442.1:c.291-58_291-33del (HRAS) NP_001123914.1:n.291-58_291-33del
NM_005343.2:c.291-58_291-33del (HRAS) NP_005334.1:n.291-58_291-33del
NM_176795.3:c.291-58_291-33del (HRAS) NP_789765.1:n.291-58_291-33del
XM_011519875.1:c.-424-4953_-424-4928del (LRRC56) XP_011518177.1:n.-424-4953_-424-4928del
XM_011519877.1:c.-162+5308_-162+5333del (LRRC56) XP_011518179.1:n.-162+5308_-162+5333del
XR_242795.1:n.490-58_490-33del (HRAS)
NM_001130442.2:c.291-58_291-33del (HRAS) NP_001123914.1:n.291-58_291-33del
NM_001318054.1:c.-29-58_-29-33del (HRAS) NP_001304983.1:n.-29-58_-29-33del
NM_005343.3:c.291-58_291-33del (HRAS) NP_005334.1:n.291-58_291-33del
NM_176795.4:c.291-58_291-33del (HRAS) NP_789765.1:n.291-58_291-33del
XM_011519875.2:c.-424-4953_-424-4928del (LRRC56) XP_011518177.1:n.-424-4953_-424-4928del
XM_011519877.2:c.-162+5308_-162+5333del (LRRC56) XP_011518179.1:n.-162+5308_-162+5333del
XM_017017167.1:c.-499-4878_-499-4853del (LRRC56) XP_016872656.1:n.-499-4878_-499-4853del
XM_017017168.1:c.-499-4878_-499-4853del (LRRC56) XP_016872657.1:n.-499-4878_-499-4853del
NM_005343.4:c.291-58_291-33del (HRAS) MANE Select NP_005334.1:n.291-58_291-33del
NM_001318054.2:c.-29-58_-29-33del (HRAS) NP_001304983.1:n.-29-58_-29-33del
NM_001130442.3:c.291-58_291-33del (HRAS) NP_001123914.1:n.291-58_291-33del
NM_176795.5:c.291-58_291-33del (HRAS) MANE Plus Clinical NP_789765.1:n.291-58_291-33del