Canonical Allele Identifier: CA180888

Linked Data

ClinVar Variation Id: 40437
dbSNP Id: rs138272051
gnomAD v2: 11-533799-T-G
gnomAD v3: 11-533799-T-G
gnomAD v4: 11-533799-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.533799T>G , CM000673.2:g.533799T>G GRCh38
NC_000011.9:g.533799T>G , CM000673.1:g.533799T>G GRCh37
NC_000011.8:g.523799T>G NCBI36
NG_007666.1:g.6752A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.257A>C (HRAS) ENSP00000380722.3:p.Asn86Thr
ENST00000417302.7:c.257A>C (HRAS) MANE Plus Clinical ENSP00000388246.1:p.Asn86Thr
ENST00000417302.6:c.257A>C (HRAS) ENSP00000388246.1:p.Asn86Thr
ENST00000462734.2:c.257A>C (HRAS) ENSP00000507303.1:p.Asn86Thr
ENST00000311189.8:c.257A>C (HRAS) MANE Select ENSP00000309845.7:p.Asn86Thr
ENST00000311189.7:c.257A>C (HRAS) ENSP00000309845.7:p.Asn86Thr
ENST00000397594.5:c.257A>C (HRAS) ENSP00000380722.1:p.Asn86Thr
ENST00000397596.6:c.257A>C (HRAS) ENSP00000380723.2:p.Asn86Thr
ENST00000417302.5:c.257A>C (HRAS) ENSP00000388246.1:p.Asn86Thr
ENST00000451590.5:c.257A>C (HRAS) ENSP00000407586.1:p.Asn86Thr
ENST00000468682.2:n.745A>C (HRAS)
ENST00000479482.1:n.178A>C (HRAS)
ENST00000493230.5:c.257A>C (HRAS) ENSP00000434023.1:p.Asn86Thr
NM_001130442.1:c.257A>C (HRAS) NP_001123914.1:p.Asn86Thr
NM_005343.2:c.257A>C (HRAS) NP_005334.1:p.Asn86Thr
NM_176795.3:c.257A>C (HRAS) NP_789765.1:p.Asn86Thr
XM_011519875.1:c.-424-4799T>G (LRRC56) XP_011518177.1:n.-424-4799T>G
XM_011519877.1:c.-162+5462T>G (LRRC56) XP_011518179.1:n.-162+5462T>G
XR_242795.1:n.456A>C (HRAS)
NM_001130442.2:c.257A>C (HRAS) NP_001123914.1:p.Asn86Thr
NM_001318054.1:c.-63A>C (HRAS) NP_001304983.1:n.-63A>C
NM_005343.3:c.257A>C (HRAS) NP_005334.1:p.Asn86Thr
NM_176795.4:c.257A>C (HRAS) NP_789765.1:p.Asn86Thr
XM_011519875.2:c.-424-4799T>G (LRRC56) XP_011518177.1:n.-424-4799T>G
XM_011519877.2:c.-162+5462T>G (LRRC56) XP_011518179.1:n.-162+5462T>G
XM_017017167.1:c.-499-4724T>G (LRRC56) XP_016872656.1:n.-499-4724T>G
XM_017017168.1:c.-499-4724T>G (LRRC56) XP_016872657.1:n.-499-4724T>G
NM_005343.4:c.257A>C (HRAS) MANE Select NP_005334.1:p.Asn86Thr
NM_001318054.2:c.-63A>C (HRAS) NP_001304983.1:n.-63A>C
NM_001130442.3:c.257A>C (HRAS) NP_001123914.1:p.Asn86Thr
NM_176795.5:c.257A>C (HRAS) MANE Plus Clinical NP_789765.1:p.Asn86Thr