Canonical Allele Identifier: CA934276206

Linked Data

dbSNP Id: rs1851155305

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532442_532465del , CM000673.2:g.532442_532465del GRCh38
NC_000011.9:g.532442_532465del , CM000673.1:g.532442_532465del GRCh37
NC_000011.8:g.522442_522465del NCBI36
NG_007666.1:g.8097_8120del

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*196_*219del (HRAS) ENSP00000380722.3:n.*196_*219del
ENST00000417302.7:c.*321_*344del (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*321_*344del
ENST00000397594.6:c.427_450del (HRAS) ENSP00000380722.2:n.427_450del
ENST00000417302.6:c.*321_*344del (HRAS) ENSP00000388246.1:n.*321_*344del
ENST00000462734.2:c.*256_*279del (HRAS) ENSP00000507303.1:n.*256_*279del
ENST00000311189.8:c.*74_*97del (HRAS) MANE Select ENSP00000309845.7:n.*74_*97del
ENST00000311189.7:c.*74_*97del (HRAS) ENSP00000309845.7:n.*74_*97del
ENST00000397594.5:c.*321_*344del (HRAS) ENSP00000380722.1:n.*321_*344del
ENST00000397596.6:c.*182_*205del (HRAS) ENSP00000380723.2:n.*182_*205del
ENST00000417302.5:c.*321_*344del (HRAS) ENSP00000388246.1:n.*321_*344del
ENST00000451590.5:c.*182_*205del (HRAS) ENSP00000407586.1:n.*182_*205del
ENST00000462734.1:n.419_442del (HRAS)
ENST00000478324.5:n.419_442del (HRAS)
ENST00000493230.5:c.*213_*236del (HRAS) ENSP00000434023.1:n.*213_*236del
NM_001130442.1:c.*182_*205del (HRAS) NP_001123914.1:n.*182_*205del
NM_005343.2:c.*74_*97del (HRAS) NP_005334.1:n.*74_*97del
NM_176795.3:c.*321_*344del (HRAS) NP_789765.1:n.*321_*344del
XM_011519875.1:c.-425+4105_-425+4128del (LRRC56) XP_011518177.1:n.-425+4105_-425+4128del
XM_011519877.1:c.-162+4105_-162+4128del (LRRC56) XP_011518179.1:n.-162+4105_-162+4128del
XR_242795.1:n.925_948del (HRAS)
NM_001130442.2:c.*182_*205del (HRAS) NP_001123914.1:n.*182_*205del
NM_001318054.1:c.*74_*97del (HRAS) NP_001304983.1:n.*74_*97del
NM_005343.3:c.*74_*97del (HRAS) NP_005334.1:n.*74_*97del
NM_176795.4:c.*321_*344del (HRAS) NP_789765.1:n.*321_*344del
XM_011519875.2:c.-425+4105_-425+4128del (LRRC56) XP_011518177.1:n.-425+4105_-425+4128del
XM_011519877.2:c.-162+4105_-162+4128del (LRRC56) XP_011518179.1:n.-162+4105_-162+4128del
XM_017017167.1:c.-500+4105_-500+4128del (LRRC56) XP_016872656.1:n.-500+4105_-500+4128del
XM_017017168.1:c.-500+4105_-500+4128del (LRRC56) XP_016872657.1:n.-500+4105_-500+4128del
NM_005343.4:c.*74_*97del (HRAS) MANE Select NP_005334.1:n.*74_*97del
NM_001318054.2:c.*74_*97del (HRAS) NP_001304983.1:n.*74_*97del
NM_001130442.3:c.*182_*205del (HRAS) NP_001123914.1:n.*182_*205del
NM_176795.5:c.*321_*344del (HRAS) MANE Plus Clinical NP_789765.1:n.*321_*344del