Canonical Allele Identifier: CA16602764

Linked Data

ClinVar Variation Id: 376318
dbSNP Id: rs121913496

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.533873C>A , CM000673.2:g.533873C>A GRCh38
NC_000011.9:g.533873C>A , CM000673.1:g.533873C>A GRCh37
NC_000011.8:g.523873C>A NCBI36
NG_007666.1:g.6678G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.183G>T (HRAS) ENSP00000380722.3:p.Gln61His
ENST00000417302.7:c.183G>T (HRAS) MANE Plus Clinical ENSP00000388246.1:p.Gln61His
ENST00000417302.6:c.183G>T (HRAS) ENSP00000388246.1:p.Gln61His
ENST00000462734.2:c.183G>T (HRAS) ENSP00000507303.1:p.Gln61His
ENST00000311189.8:c.183G>T (HRAS) MANE Select ENSP00000309845.7:p.Gln61His
ENST00000311189.7:c.183G>T (HRAS) ENSP00000309845.7:p.Gln61His
ENST00000397594.5:c.183G>T (HRAS) ENSP00000380722.1:p.Gln61His
ENST00000397596.6:c.183G>T (HRAS) ENSP00000380723.2:p.Gln61His
ENST00000417302.5:c.183G>T (HRAS) ENSP00000388246.1:p.Gln61His
ENST00000451590.5:c.183G>T (HRAS) ENSP00000407586.1:p.Gln61His
ENST00000468682.2:n.671G>T (HRAS)
ENST00000479482.1:n.104G>T (HRAS)
ENST00000493230.5:c.183G>T (HRAS) ENSP00000434023.1:p.Gln61His
NM_001130442.1:c.183G>T (HRAS) NP_001123914.1:p.Gln61His
NM_005343.2:c.183G>T (HRAS) NP_005334.1:p.Gln61His
NM_176795.3:c.183G>T (HRAS) NP_789765.1:p.Gln61His
XM_011519875.1:c.-424-4725C>A (LRRC56) XP_011518177.1:n.-424-4725C>A
XM_011519877.1:c.-162+5536C>A (LRRC56) XP_011518179.1:n.-162+5536C>A
XR_242795.1:n.382G>T (HRAS)
NM_001130442.2:c.183G>T (HRAS) NP_001123914.1:p.Gln61His
NM_001318054.1:c.-137G>T (HRAS) NP_001304983.1:n.-137G>T
NM_005343.3:c.183G>T (HRAS) NP_005334.1:p.Gln61His
NM_176795.4:c.183G>T (HRAS) NP_789765.1:p.Gln61His
XM_011519875.2:c.-424-4725C>A (LRRC56) XP_011518177.1:n.-424-4725C>A
XM_011519877.2:c.-162+5536C>A (LRRC56) XP_011518179.1:n.-162+5536C>A
XM_017017167.1:c.-499-4650C>A (LRRC56) XP_016872656.1:n.-499-4650C>A
XM_017017168.1:c.-499-4650C>A (LRRC56) XP_016872657.1:n.-499-4650C>A
NM_005343.4:c.183G>T (HRAS) MANE Select NP_005334.1:p.Gln61His
NM_001318054.2:c.-137G>T (HRAS) NP_001304983.1:n.-137G>T
NM_001130442.3:c.183G>T (HRAS) NP_001123914.1:p.Gln61His
NM_176795.5:c.183G>T (HRAS) MANE Plus Clinical NP_789765.1:p.Gln61His