Canonical Allele Identifier: CA5779258

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.533311_533330del , CM000673.2:g.533311_533330del GRCh38
NC_000011.9:g.533311_533330del , CM000673.1:g.533311_533330del GRCh37
NC_000011.8:g.523311_523330del NCBI36
NG_007666.1:g.7230_7249del

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.488_507del (HRAS) ENSP00000380722.3:p.Leu163HisfsTer10
ENST00000417302.7:c.488_507del (HRAS) MANE Plus Clinical ENSP00000388246.1:p.Leu163HisfsTer30
ENST00000397594.6:c.206_225del (HRAS) ENSP00000380722.2:p.Leu69HisfsTer10
ENST00000417302.6:c.488_507del (HRAS) ENSP00000388246.1:p.Leu163HisfsTer30
ENST00000462734.2:c.*18_*37del (HRAS) ENSP00000507303.1:n.*18_*37del
ENST00000311189.8:c.450+132_450+151del (HRAS) MANE Select ENSP00000309845.7:n.450+132_450+151del
ENST00000311189.7:c.450+132_450+151del (HRAS) ENSP00000309845.7:n.450+132_450+151del
ENST00000397594.5:c.488_507del (HRAS) ENSP00000380722.1:p.Leu163HisfsTer30
ENST00000397596.6:c.450+132_450+151del (HRAS) ENSP00000380723.2:n.450+132_450+151del
ENST00000417302.5:c.488_507del (HRAS) ENSP00000388246.1:p.Leu163HisfsTer30
ENST00000451590.5:c.450+132_450+151del (HRAS) ENSP00000407586.1:n.450+132_450+151del
ENST00000462734.1:n.181_200del (HRAS)
ENST00000478324.5:n.198_217del (HRAS)
ENST00000479482.1:n.371+132_371+151del (HRAS)
ENST00000493230.5:c.488_507del (HRAS) ENSP00000434023.1:p.Leu163HisfsTer30
NM_001130442.1:c.450+132_450+151del (HRAS) NP_001123914.1:n.450+132_450+151del
NM_005343.2:c.450+132_450+151del (HRAS) NP_005334.1:n.450+132_450+151del
NM_176795.3:c.488_507del (HRAS) NP_789765.1:p.Leu163HisfsTer30
XM_011519875.1:c.-425+4974_-425+4993del (LRRC56) XP_011518177.1:n.-425+4974_-425+4993del
XM_011519877.1:c.-162+4974_-162+4993del (LRRC56) XP_011518179.1:n.-162+4974_-162+4993del
XR_242795.1:n.687_706del (HRAS)
NM_001130442.2:c.450+132_450+151del (HRAS) NP_001123914.1:n.450+132_450+151del
NM_001318054.1:c.169_188del (HRAS) NP_001304983.1:p.Ser57MetfsTer2
NM_005343.3:c.450+132_450+151del (HRAS) NP_005334.1:n.450+132_450+151del
NM_176795.4:c.488_507del (HRAS) NP_789765.1:p.Leu163HisfsTer30
XM_011519875.2:c.-425+4974_-425+4993del (LRRC56) XP_011518177.1:n.-425+4974_-425+4993del
XM_011519877.2:c.-162+4974_-162+4993del (LRRC56) XP_011518179.1:n.-162+4974_-162+4993del
XM_017017167.1:c.-500+4974_-500+4993del (LRRC56) XP_016872656.1:n.-500+4974_-500+4993del
XM_017017168.1:c.-500+4974_-500+4993del (LRRC56) XP_016872657.1:n.-500+4974_-500+4993del
NM_005343.4:c.450+132_450+151del (HRAS) MANE Select NP_005334.1:n.450+132_450+151del
NM_001318054.2:c.169_188del (HRAS) NP_001304983.1:p.Ser57MetfsTer2
NM_001130442.3:c.450+132_450+151del (HRAS) NP_001123914.1:n.450+132_450+151del
NM_176795.5:c.488_507del (HRAS) MANE Plus Clinical NP_789765.1:p.Leu163HisfsTer30