Canonical Allele Identifier: CA1947140599

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532471_532474delinsTTCC , CM000673.2:g.532471_532474delinsTTCC GRCh38
NC_000011.9:g.532471_532474delinsTTCC , CM000673.1:g.532471_532474delinsTTCC GRCh37
NC_000011.8:g.522471_522474delinsTTCC NCBI36
NG_007666.1:g.8077_8080delinsGGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*176_*179delinsGGAA (HRAS) ENSP00000380722.3:n.*176_*179delinsGGAA
ENST00000417302.7:c.*301_*304delinsGGAA (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*301_*304delinsGGAA
ENST00000397594.6:c.407_410delinsGGAA (HRAS) ENSP00000380722.2:n.407_410delinsGGAA
ENST00000417302.6:c.*301_*304delinsGGAA (HRAS) ENSP00000388246.1:n.*301_*304delinsGGAA
ENST00000462734.2:c.*236_*239delinsGGAA (HRAS) ENSP00000507303.1:n.*236_*239delinsGGAA
ENST00000311189.8:c.*54_*57delinsGGAA (HRAS) MANE Select ENSP00000309845.7:n.*54_*57delinsGGAA
ENST00000311189.7:c.*54_*57delinsGGAA (HRAS) ENSP00000309845.7:n.*54_*57delinsGGAA
ENST00000397594.5:c.*301_*304delinsGGAA (HRAS) ENSP00000380722.1:n.*301_*304delinsGGAA
ENST00000397596.6:c.*162_*165delinsGGAA (HRAS) ENSP00000380723.2:n.*162_*165delinsGGAA
ENST00000417302.5:c.*301_*304delinsGGAA (HRAS) ENSP00000388246.1:n.*301_*304delinsGGAA
ENST00000451590.5:c.*162_*165delinsGGAA (HRAS) ENSP00000407586.1:n.*162_*165delinsGGAA
ENST00000462734.1:n.399_402delinsGGAA (HRAS)
ENST00000478324.5:n.399_402delinsGGAA (HRAS)
ENST00000493230.5:c.*193_*196delinsGGAA (HRAS) ENSP00000434023.1:n.*193_*196delinsGGAA
NM_001130442.1:c.*162_*165delinsGGAA (HRAS) NP_001123914.1:n.*162_*165delinsGGAA
NM_005343.2:c.*54_*57delinsGGAA (HRAS) NP_005334.1:n.*54_*57delinsGGAA
NM_176795.3:c.*301_*304delinsGGAA (HRAS) NP_789765.1:n.*301_*304delinsGGAA
XM_011519875.1:c.-425+4134_-425+4137delinsTTCC (LRRC56) XP_011518177.1:n.-425+4134_-425+4137delinsTTCC
XM_011519877.1:c.-162+4134_-162+4137delinsTTCC (LRRC56) XP_011518179.1:n.-162+4134_-162+4137delinsTTCC
XR_242795.1:n.905_908delinsGGAA (HRAS)
NM_001130442.2:c.*162_*165delinsGGAA (HRAS) NP_001123914.1:n.*162_*165delinsGGAA
NM_001318054.1:c.*54_*57delinsGGAA (HRAS) NP_001304983.1:n.*54_*57delinsGGAA
NM_005343.3:c.*54_*57delinsGGAA (HRAS) NP_005334.1:n.*54_*57delinsGGAA
NM_176795.4:c.*301_*304delinsGGAA (HRAS) NP_789765.1:n.*301_*304delinsGGAA
XM_011519875.2:c.-425+4134_-425+4137delinsTTCC (LRRC56) XP_011518177.1:n.-425+4134_-425+4137delinsTTCC
XM_011519877.2:c.-162+4134_-162+4137delinsTTCC (LRRC56) XP_011518179.1:n.-162+4134_-162+4137delinsTTCC
XM_017017167.1:c.-500+4134_-500+4137delinsTTCC (LRRC56) XP_016872656.1:n.-500+4134_-500+4137delinsTTCC
XM_017017168.1:c.-500+4134_-500+4137delinsTTCC (LRRC56) XP_016872657.1:n.-500+4134_-500+4137delinsTTCC
NM_005343.4:c.*54_*57delinsGGAA (HRAS) MANE Select NP_005334.1:n.*54_*57delinsGGAA
NM_001318054.2:c.*54_*57delinsGGAA (HRAS) NP_001304983.1:n.*54_*57delinsGGAA
NM_001130442.3:c.*162_*165delinsGGAA (HRAS) NP_001123914.1:n.*162_*165delinsGGAA
NM_176795.5:c.*301_*304delinsGGAA (HRAS) MANE Plus Clinical NP_789765.1:n.*301_*304delinsGGAA