Canonical Allele Identifier: CA596781464

Linked Data

dbSNP Id: rs1405797450
gnomAD v2: 11-532455-C-T
gnomAD v3: 11-532455-C-T
gnomAD v4: 11-532455-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532455C>T , CM000673.2:g.532455C>T GRCh38
NC_000011.9:g.532455C>T , CM000673.1:g.532455C>T GRCh37
NC_000011.8:g.522455C>T NCBI36
NG_007666.1:g.8096G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*195G>A (HRAS) ENSP00000380722.3:n.*195G>A
ENST00000417302.7:c.*320G>A (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*320G>A
ENST00000397594.6:c.426G>A (HRAS) ENSP00000380722.2:n.426G>A
ENST00000417302.6:c.*320G>A (HRAS) ENSP00000388246.1:n.*320G>A
ENST00000462734.2:c.*255G>A (HRAS) ENSP00000507303.1:n.*255G>A
ENST00000311189.8:c.*73G>A (HRAS) MANE Select ENSP00000309845.7:n.*73G>A
ENST00000311189.7:c.*73G>A (HRAS) ENSP00000309845.7:n.*73G>A
ENST00000397594.5:c.*320G>A (HRAS) ENSP00000380722.1:n.*320G>A
ENST00000397596.6:c.*181G>A (HRAS) ENSP00000380723.2:n.*181G>A
ENST00000417302.5:c.*320G>A (HRAS) ENSP00000388246.1:n.*320G>A
ENST00000451590.5:c.*181G>A (HRAS) ENSP00000407586.1:n.*181G>A
ENST00000462734.1:n.418G>A (HRAS)
ENST00000478324.5:n.418G>A (HRAS)
ENST00000493230.5:c.*212G>A (HRAS) ENSP00000434023.1:n.*212G>A
NM_001130442.1:c.*181G>A (HRAS) NP_001123914.1:n.*181G>A
NM_005343.2:c.*73G>A (HRAS) NP_005334.1:n.*73G>A
NM_176795.3:c.*320G>A (HRAS) NP_789765.1:n.*320G>A
XM_011519875.1:c.-425+4118C>T (LRRC56) XP_011518177.1:n.-425+4118C>T
XM_011519877.1:c.-162+4118C>T (LRRC56) XP_011518179.1:n.-162+4118C>T
XR_242795.1:n.924G>A (HRAS)
NM_001130442.2:c.*181G>A (HRAS) NP_001123914.1:n.*181G>A
NM_001318054.1:c.*73G>A (HRAS) NP_001304983.1:n.*73G>A
NM_005343.3:c.*73G>A (HRAS) NP_005334.1:n.*73G>A
NM_176795.4:c.*320G>A (HRAS) NP_789765.1:n.*320G>A
XM_011519875.2:c.-425+4118C>T (LRRC56) XP_011518177.1:n.-425+4118C>T
XM_011519877.2:c.-162+4118C>T (LRRC56) XP_011518179.1:n.-162+4118C>T
XM_017017167.1:c.-500+4118C>T (LRRC56) XP_016872656.1:n.-500+4118C>T
XM_017017168.1:c.-500+4118C>T (LRRC56) XP_016872657.1:n.-500+4118C>T
NM_005343.4:c.*73G>A (HRAS) MANE Select NP_005334.1:n.*73G>A
NM_001318054.2:c.*73G>A (HRAS) NP_001304983.1:n.*73G>A
NM_001130442.3:c.*181G>A (HRAS) NP_001123914.1:n.*181G>A
NM_176795.5:c.*320G>A (HRAS) MANE Plus Clinical NP_789765.1:n.*320G>A