Canonical Allele Identifier: CA295247

Linked Data

ClinVar Variation Id: 12606
dbSNP Id: rs104894228

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.534286C>A , CM000673.2:g.534286C>A GRCh38
NC_000011.9:g.534286C>A , CM000673.1:g.534286C>A GRCh37
NC_000011.8:g.524286C>A NCBI36
NG_007666.1:g.6265G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000311189.8:c.37G>T MANE Select ENSP00000309845.7:p.Gly13Cys
ENST00000311189.7:c.37G>T ENSP00000309845.7:p.Gly13Cys
ENST00000397594.5:c.37G>T ENSP00000380722.1:p.Gly13Cys
ENST00000397596.6:c.37G>T ENSP00000380723.2:p.Gly13Cys
ENST00000417302.5:c.37G>T ENSP00000388246.1:p.Gly13Cys
ENST00000451590.5:c.37G>T ENSP00000407586.1:p.Gly13Cys
ENST00000468682.2:n.525G>T
ENST00000482021.1:n.160G>T
ENST00000493230.5:c.37G>T ENSP00000434023.1:p.Gly13Cys
NM_001130442.1:c.37G>T (HRAS) NP_001123914.1:p.Gly13Cys
NM_005343.2:c.37G>T (HRAS) NP_005334.1:p.Gly13Cys
NM_176795.3:c.37G>T (HRAS) NP_789765.1:p.Gly13Cys
XM_011519875.1:c.-424-4312C>A (LRRC56) XP_011518177.1:p.=
XM_011519877.1:c.-161-5294C>A (LRRC56) XP_011518179.1:p.=
XR_242795.1:n.236G>T (HRAS)
NM_001130442.2:c.37G>T (HRAS) NP_001123914.1:p.Gly13Cys
NM_001318054.1:c.-283G>T (HRAS) NP_001304983.1:p.=
NM_005343.3:c.37G>T (HRAS) NP_005334.1:p.Gly13Cys
NM_176795.4:c.37G>T (HRAS) NP_789765.1:p.Gly13Cys
XM_011519875.2:c.-424-4312C>A (LRRC56) XP_011518177.1:p.=
XM_011519877.2:c.-161-5294C>A (LRRC56) XP_011518179.1:p.=
XM_017017167.1:c.-499-4237C>A (LRRC56) XP_016872656.1:p.=
XM_017017168.1:c.-499-4237C>A (LRRC56) XP_016872657.1:p.=
NM_005343.4:c.37G>T (HRAS) MANE Select NP_005334.1:p.Gly13Cys
NM_001318054.2:c.-283G>T (HRAS) NP_001304983.1:p.=
NM_001130442.3:c.37G>T (HRAS) NP_001123914.1:p.Gly13Cys
NM_176795.5:c.37G>T (HRAS) NP_789765.1:p.Gly13Cys