Canonical Allele Identifier: CA596781462

Linked Data

dbSNP Id: rs1186214149

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532447_532462del , CM000673.2:g.532447_532462del GRCh38
NC_000011.9:g.532447_532462del , CM000673.1:g.532447_532462del GRCh37
NC_000011.8:g.522447_522462del NCBI36
NG_007666.1:g.8098_8113del

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*197_*212del (HRAS) ENSP00000380722.3:n.*197_*212del
ENST00000417302.7:c.*322_*337del (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*322_*337del
ENST00000397594.6:c.428_443del (HRAS) ENSP00000380722.2:n.428_443del
ENST00000417302.6:c.*322_*337del (HRAS) ENSP00000388246.1:n.*322_*337del
ENST00000462734.2:c.*257_*272del (HRAS) ENSP00000507303.1:n.*257_*272del
ENST00000311189.8:c.*75_*90del (HRAS) MANE Select ENSP00000309845.7:n.*75_*90del
ENST00000311189.7:c.*75_*90del (HRAS) ENSP00000309845.7:n.*75_*90del
ENST00000397594.5:c.*322_*337del (HRAS) ENSP00000380722.1:n.*322_*337del
ENST00000397596.6:c.*183_*198del (HRAS) ENSP00000380723.2:n.*183_*198del
ENST00000417302.5:c.*322_*337del (HRAS) ENSP00000388246.1:n.*322_*337del
ENST00000451590.5:c.*183_*198del (HRAS) ENSP00000407586.1:n.*183_*198del
ENST00000462734.1:n.420_435del (HRAS)
ENST00000478324.5:n.420_435del (HRAS)
ENST00000493230.5:c.*214_*229del (HRAS) ENSP00000434023.1:n.*214_*229del
NM_001130442.1:c.*183_*198del (HRAS) NP_001123914.1:n.*183_*198del
NM_005343.2:c.*75_*90del (HRAS) NP_005334.1:n.*75_*90del
NM_176795.3:c.*322_*337del (HRAS) NP_789765.1:n.*322_*337del
XM_011519875.1:c.-425+4110_-425+4125del (LRRC56) XP_011518177.1:n.-425+4110_-425+4125del
XM_011519877.1:c.-162+4110_-162+4125del (LRRC56) XP_011518179.1:n.-162+4110_-162+4125del
XR_242795.1:n.926_941del (HRAS)
NM_001130442.2:c.*183_*198del (HRAS) NP_001123914.1:n.*183_*198del
NM_001318054.1:c.*75_*90del (HRAS) NP_001304983.1:n.*75_*90del
NM_005343.3:c.*75_*90del (HRAS) NP_005334.1:n.*75_*90del
NM_176795.4:c.*322_*337del (HRAS) NP_789765.1:n.*322_*337del
XM_011519875.2:c.-425+4110_-425+4125del (LRRC56) XP_011518177.1:n.-425+4110_-425+4125del
XM_011519877.2:c.-162+4110_-162+4125del (LRRC56) XP_011518179.1:n.-162+4110_-162+4125del
XM_017017167.1:c.-500+4110_-500+4125del (LRRC56) XP_016872656.1:n.-500+4110_-500+4125del
XM_017017168.1:c.-500+4110_-500+4125del (LRRC56) XP_016872657.1:n.-500+4110_-500+4125del
NM_005343.4:c.*75_*90del (HRAS) MANE Select NP_005334.1:n.*75_*90del
NM_001318054.2:c.*75_*90del (HRAS) NP_001304983.1:n.*75_*90del
NM_001130442.3:c.*183_*198del (HRAS) NP_001123914.1:n.*183_*198del
NM_176795.5:c.*322_*337del (HRAS) MANE Plus Clinical NP_789765.1:n.*322_*337del