Canonical Allele Identifier: CA1947140945

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532620G= , CM000673.2:g.532620G= GRCh38
NC_000011.9:g.532620G= , CM000673.1:g.532620G= GRCh37
NC_000011.8:g.522620G= NCBI36
NG_007666.1:g.7931C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*30C= (HRAS) ENSP00000380722.3:n.*30C=
ENST00000417302.7:c.*155C= (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*155C=
ENST00000397594.6:c.261C= (HRAS) ENSP00000380722.2:n.261C=
ENST00000417302.6:c.*155C= (HRAS) ENSP00000388246.1:n.*155C=
ENST00000462734.2:c.*187+11C= (HRAS) ENSP00000507303.1:n.*187+11C=
ENST00000311189.8:c.*5+11C= (HRAS) MANE Select ENSP00000309845.7:n.*5+11C=
ENST00000311189.7:c.*5+11C= (HRAS) ENSP00000309845.7:n.*5+11C=
ENST00000397594.5:c.*155C= (HRAS) ENSP00000380722.1:n.*155C=
ENST00000397596.6:c.*16C= (HRAS) ENSP00000380723.2:n.*16C=
ENST00000417302.5:c.*155C= (HRAS) ENSP00000388246.1:n.*155C=
ENST00000451590.5:c.*16C= (HRAS) ENSP00000407586.1:n.*16C=
ENST00000462734.1:n.350+11C= (HRAS)
ENST00000478324.5:n.253C= (HRAS)
ENST00000493230.5:c.*144+11C= (HRAS) ENSP00000434023.1:n.*144+11C=
NM_001130442.1:c.*16C= (HRAS) NP_001123914.1:n.*16C=
NM_005343.2:c.*5+11C= (HRAS) NP_005334.1:n.*5+11C=
NM_176795.3:c.*155C= (HRAS) NP_789765.1:n.*155C=
XM_011519875.1:c.-425+4283G= (LRRC56) XP_011518177.1:n.-425+4283G=
XM_011519877.1:c.-162+4283G= (LRRC56) XP_011518179.1:n.-162+4283G=
XR_242795.1:n.856+11C= (HRAS)
NM_001130442.2:c.*16C= (HRAS) NP_001123914.1:n.*16C=
NM_001318054.1:c.*5+11C= (HRAS) NP_001304983.1:n.*5+11C=
NM_005343.3:c.*5+11C= (HRAS) NP_005334.1:n.*5+11C=
NM_176795.4:c.*155C= (HRAS) NP_789765.1:n.*155C=
XM_011519875.2:c.-425+4283G= (LRRC56) XP_011518177.1:n.-425+4283G=
XM_011519877.2:c.-162+4283G= (LRRC56) XP_011518179.1:n.-162+4283G=
XM_017017167.1:c.-500+4283G= (LRRC56) XP_016872656.1:n.-500+4283G=
XM_017017168.1:c.-500+4283G= (LRRC56) XP_016872657.1:n.-500+4283G=
NM_005343.4:c.*5+11C= (HRAS) MANE Select NP_005334.1:n.*5+11C=
NM_001318054.2:c.*5+11C= (HRAS) NP_001304983.1:n.*5+11C=
NM_001130442.3:c.*16C= (HRAS) NP_001123914.1:n.*16C=
NM_176795.5:c.*155C= (HRAS) MANE Plus Clinical NP_789765.1:n.*155C=