Canonical Allele Identifier: CA1947140375

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532364A= , CM000673.2:g.532364A= GRCh38
NC_000011.9:g.532364A= , CM000673.1:g.532364A= GRCh37
NC_000011.8:g.522364A= NCBI36
NG_007666.1:g.8187T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*286T= (HRAS) ENSP00000380722.3:n.*286T=
ENST00000417302.7:c.*411T= (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*411T=
ENST00000397594.6:c.517T= (HRAS) ENSP00000380722.2:n.517T=
ENST00000417302.6:c.*411T= (HRAS) ENSP00000388246.1:n.*411T=
ENST00000462734.2:c.*346T= (HRAS) ENSP00000507303.1:n.*346T=
ENST00000311189.8:c.*164T= (HRAS) MANE Select ENSP00000309845.7:n.*164T=
ENST00000397594.5:c.*411T= (HRAS) ENSP00000380722.1:n.*411T=
ENST00000397596.6:c.*272T= (HRAS) ENSP00000380723.2:n.*272T=
ENST00000417302.5:c.*411T= (HRAS) ENSP00000388246.1:n.*411T=
ENST00000451590.5:c.*272T= (HRAS) ENSP00000407586.1:n.*272T=
ENST00000462734.1:n.509T= (HRAS)
ENST00000478324.5:n.509T= (HRAS)
ENST00000493230.5:c.*303T= (HRAS) ENSP00000434023.1:n.*303T=
NM_001130442.1:c.*272T= (HRAS) NP_001123914.1:n.*272T=
NM_005343.2:c.*164T= (HRAS) NP_005334.1:n.*164T=
NM_176795.3:c.*411T= (HRAS) NP_789765.1:n.*411T=
XM_011519875.1:c.-425+4027A= (LRRC56) XP_011518177.1:n.-425+4027A=
XM_011519877.1:c.-162+4027A= (LRRC56) XP_011518179.1:n.-162+4027A=
XR_242795.1:n.1015T= (HRAS)
NM_001130442.2:c.*272T= (HRAS) NP_001123914.1:n.*272T=
NM_001318054.1:c.*164T= (HRAS) NP_001304983.1:n.*164T=
NM_005343.3:c.*164T= (HRAS) NP_005334.1:n.*164T=
NM_176795.4:c.*411T= (HRAS) NP_789765.1:n.*411T=
XM_011519875.2:c.-425+4027A= (LRRC56) XP_011518177.1:n.-425+4027A=
XM_011519877.2:c.-162+4027A= (LRRC56) XP_011518179.1:n.-162+4027A=
XM_017017167.1:c.-500+4027A= (LRRC56) XP_016872656.1:n.-500+4027A=
XM_017017168.1:c.-500+4027A= (LRRC56) XP_016872657.1:n.-500+4027A=
NM_005343.4:c.*164T= (HRAS) MANE Select NP_005334.1:n.*164T=
NM_001318054.2:c.*164T= (HRAS) NP_001304983.1:n.*164T=
NM_001130442.3:c.*272T= (HRAS) NP_001123914.1:n.*272T=
NM_176795.5:c.*411T= (HRAS) MANE Plus Clinical NP_789765.1:n.*411T=