Canonical Allele Identifier: CA341206

Linked Data

ClinVar Variation Id: 12610
ClinVar RCV Id: RCV000013444
dbSNP Id: rs121917758

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.533883G>A , CM000673.2:g.533883G>A GRCh38
NC_000011.9:g.533883G>A , CM000673.1:g.533883G>A GRCh37
NC_000011.8:g.523883G>A NCBI36
NG_007666.1:g.6668C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000311189.8:c.173C>T MANE Select ENSP00000309845.7:p.Thr58Ile
ENST00000311189.7:c.173C>T ENSP00000309845.7:p.Thr58Ile
ENST00000397594.5:c.173C>T ENSP00000380722.1:p.Thr58Ile
ENST00000397596.6:c.173C>T ENSP00000380723.2:p.Thr58Ile
ENST00000417302.5:c.173C>T ENSP00000388246.1:p.Thr58Ile
ENST00000451590.5:c.173C>T ENSP00000407586.1:p.Thr58Ile
ENST00000468682.2:n.661C>T
ENST00000479482.1:n.94C>T
ENST00000493230.5:c.173C>T ENSP00000434023.1:p.Thr58Ile
NM_001130442.1:c.173C>T (HRAS) NP_001123914.1:p.Thr58Ile
NM_005343.2:c.173C>T (HRAS) NP_005334.1:p.Thr58Ile
NM_176795.3:c.173C>T (HRAS) NP_789765.1:p.Thr58Ile
XM_011519875.1:c.-424-4715G>A (LRRC56) XP_011518177.1:p.=
XM_011519877.1:c.-162+5546G>A (LRRC56) XP_011518179.1:p.=
XR_242795.1:n.372C>T (HRAS)
NM_001130442.2:c.173C>T (HRAS) NP_001123914.1:p.Thr58Ile
NM_001318054.1:c.-147C>T (HRAS) NP_001304983.1:p.=
NM_005343.3:c.173C>T (HRAS) NP_005334.1:p.Thr58Ile
NM_176795.4:c.173C>T (HRAS) NP_789765.1:p.Thr58Ile
XM_011519875.2:c.-424-4715G>A (LRRC56) XP_011518177.1:p.=
XM_011519877.2:c.-162+5546G>A (LRRC56) XP_011518179.1:p.=
XM_017017167.1:c.-499-4640G>A (LRRC56) XP_016872656.1:p.=
XM_017017168.1:c.-499-4640G>A (LRRC56) XP_016872657.1:p.=
NM_005343.4:c.173C>T (HRAS) MANE Select NP_005334.1:p.Thr58Ile
NM_001318054.2:c.-147C>T (HRAS) NP_001304983.1:p.=
NM_001130442.3:c.173C>T (HRAS) NP_001123914.1:p.Thr58Ile
NM_176795.5:c.173C>T (HRAS) NP_789765.1:p.Thr58Ile