Canonical Allele Identifier: CA2580083836

Linked Data

ClinVar Variation Id: 2014533
ClinVar RCV Id: RCV002861544

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532675_532677del , CM000673.2:g.532675_532677del GRCh38
NC_000011.9:g.532675_532677del , CM000673.1:g.532675_532677del GRCh37
NC_000011.8:g.522675_522677del NCBI36
NG_007666.1:g.7874_7876del

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*20-47_*20-45del (HRAS) ENSP00000380722.3:n.*20-47_*20-45del
ENST00000417302.7:c.*98_*100del (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*98_*100del
ENST00000397594.6:c.251-47_251-45del (HRAS) ENSP00000380722.2:n.251-47_251-45del
ENST00000417302.6:c.*98_*100del (HRAS) ENSP00000388246.1:n.*98_*100del
ENST00000462734.2:c.*141_*143del (HRAS) ENSP00000507303.1:n.*141_*143del
ENST00000311189.8:c.529_531del (HRAS) MANE Select ENSP00000309845.7:p.Ser177del
ENST00000311189.7:c.529_531del (HRAS) ENSP00000309845.7:p.Ser177del
ENST00000397594.5:c.*98_*100del (HRAS) ENSP00000380722.1:n.*98_*100del
ENST00000397596.6:c.529_531del (HRAS) ENSP00000380723.2:p.Ser177del
ENST00000417302.5:c.*98_*100del (HRAS) ENSP00000388246.1:n.*98_*100del
ENST00000451590.5:c.529_531del (HRAS) ENSP00000407586.1:p.Ser177del
ENST00000462734.1:n.304_306del (HRAS)
ENST00000478324.5:n.243-47_243-45del (HRAS)
ENST00000479482.1:n.450_452del (HRAS)
ENST00000493230.5:c.*98_*100del (HRAS) ENSP00000434023.1:n.*98_*100del
NM_001130442.1:c.529_531del (HRAS) NP_001123914.1:p.Ser177del
NM_005343.2:c.529_531del (HRAS) NP_005334.1:p.Ser177del
NM_176795.3:c.*98_*100del (HRAS) NP_789765.1:n.*98_*100del
XM_011519875.1:c.-425+4338_-425+4340del (LRRC56) XP_011518177.1:n.-425+4338_-425+4340del
XM_011519877.1:c.-162+4338_-162+4340del (LRRC56) XP_011518179.1:n.-162+4338_-162+4340del
XR_242795.1:n.810_812del (HRAS)
NM_001130442.2:c.529_531del (HRAS) NP_001123914.1:p.Ser177del
NM_001318054.1:c.292_294del (HRAS) NP_001304983.1:p.Ser98del
NM_005343.3:c.529_531del (HRAS) NP_005334.1:p.Ser177del
NM_176795.4:c.*98_*100del (HRAS) NP_789765.1:n.*98_*100del
XM_011519875.2:c.-425+4338_-425+4340del (LRRC56) XP_011518177.1:n.-425+4338_-425+4340del
XM_011519877.2:c.-162+4338_-162+4340del (LRRC56) XP_011518179.1:n.-162+4338_-162+4340del
XM_017017167.1:c.-500+4338_-500+4340del (LRRC56) XP_016872656.1:n.-500+4338_-500+4340del
XM_017017168.1:c.-500+4338_-500+4340del (LRRC56) XP_016872657.1:n.-500+4338_-500+4340del
NM_005343.4:c.529_531del (HRAS) MANE Select NP_005334.1:p.Ser177del
NM_001318054.2:c.292_294del (HRAS) NP_001304983.1:p.Ser98del
NM_001130442.3:c.529_531del (HRAS) NP_001123914.1:p.Ser177del
NM_176795.5:c.*98_*100del (HRAS) MANE Plus Clinical NP_789765.1:n.*98_*100del