Canonical Allele Identifier: CA1947141370

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532744A= , CM000673.2:g.532744A= GRCh38
NC_000011.9:g.532744A= , CM000673.1:g.532744A= GRCh37
NC_000011.8:g.522744A= NCBI36
NG_007666.1:g.7807T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*20-114T= (HRAS) ENSP00000380722.3:n.*20-114T=
ENST00000417302.7:c.*31T= (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*31T=
ENST00000397594.6:c.251-114T= (HRAS) ENSP00000380722.2:n.251-114T=
ENST00000417302.6:c.*31T= (HRAS) ENSP00000388246.1:n.*31T=
ENST00000462734.2:c.*74T= (HRAS) ENSP00000507303.1:n.*74T=
ENST00000311189.8:c.462T= (HRAS) MANE Select ENSP00000309845.7:p.Asp154=
ENST00000311189.7:c.462T= (HRAS) ENSP00000309845.7:p.Asp154=
ENST00000397594.5:c.*31T= (HRAS) ENSP00000380722.1:n.*31T=
ENST00000397596.6:c.462T= (HRAS) ENSP00000380723.2:p.Asp154=
ENST00000417302.5:c.*31T= (HRAS) ENSP00000388246.1:n.*31T=
ENST00000451590.5:c.462T= (HRAS) ENSP00000407586.1:p.Asp154=
ENST00000462734.1:n.237T= (HRAS)
ENST00000478324.5:n.243-114T= (HRAS)
ENST00000479482.1:n.383T= (HRAS)
ENST00000493230.5:c.*31T= (HRAS) ENSP00000434023.1:n.*31T=
NM_001130442.1:c.462T= (HRAS) NP_001123914.1:p.Asp154=
NM_005343.2:c.462T= (HRAS) NP_005334.1:p.Asp154=
NM_176795.3:c.*31T= (HRAS) NP_789765.1:n.*31T=
XM_011519875.1:c.-425+4407A= (LRRC56) XP_011518177.1:n.-425+4407A=
XM_011519877.1:c.-162+4407A= (LRRC56) XP_011518179.1:n.-162+4407A=
XR_242795.1:n.743T= (HRAS)
NM_001130442.2:c.462T= (HRAS) NP_001123914.1:p.Asp154=
NM_001318054.1:c.225T= (HRAS) NP_001304983.1:p.Asp75=
NM_005343.3:c.462T= (HRAS) NP_005334.1:p.Asp154=
NM_176795.4:c.*31T= (HRAS) NP_789765.1:n.*31T=
XM_011519875.2:c.-425+4407A= (LRRC56) XP_011518177.1:n.-425+4407A=
XM_011519877.2:c.-162+4407A= (LRRC56) XP_011518179.1:n.-162+4407A=
XM_017017167.1:c.-500+4407A= (LRRC56) XP_016872656.1:n.-500+4407A=
XM_017017168.1:c.-500+4407A= (LRRC56) XP_016872657.1:n.-500+4407A=
NM_005343.4:c.462T= (HRAS) MANE Select NP_005334.1:p.Asp154=
NM_001318054.2:c.225T= (HRAS) NP_001304983.1:p.Asp75=
NM_001130442.3:c.462T= (HRAS) NP_001123914.1:p.Asp154=
NM_176795.5:c.*31T= (HRAS) MANE Plus Clinical NP_789765.1:n.*31T=