Canonical Allele Identifier: CA2611691909

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532707_532716del , CM000673.2:g.532707_532716del GRCh38
NC_000011.9:g.532707_532716del , CM000673.1:g.532707_532716del GRCh37
NC_000011.8:g.522707_522716del NCBI36
NG_007666.1:g.7835_7844del

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*20-86_*20-77del (HRAS) ENSP00000380722.3:n.*20-86_*20-77del
ENST00000417302.7:c.*59_*68del (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*59_*68del
ENST00000397594.6:c.251-86_251-77del (HRAS) ENSP00000380722.2:n.251-86_251-77del
ENST00000417302.6:c.*59_*68del (HRAS) ENSP00000388246.1:n.*59_*68del
ENST00000462734.2:c.*102_*111del (HRAS) ENSP00000507303.1:n.*102_*111del
ENST00000311189.8:c.490_499del (HRAS) MANE Select ENSP00000309845.7:p.Arg164SerfsTer5
ENST00000311189.7:c.490_499del (HRAS) ENSP00000309845.7:p.Arg164SerfsTer5
ENST00000397594.5:c.*59_*68del (HRAS) ENSP00000380722.1:n.*59_*68del
ENST00000397596.6:c.490_499del (HRAS) ENSP00000380723.2:p.Arg164SerfsTer5
ENST00000417302.5:c.*59_*68del (HRAS) ENSP00000388246.1:n.*59_*68del
ENST00000451590.5:c.490_499del (HRAS) ENSP00000407586.1:p.Arg164SerfsTer5
ENST00000462734.1:n.265_274del (HRAS)
ENST00000478324.5:n.243-86_243-77del (HRAS)
ENST00000479482.1:n.411_420del (HRAS)
ENST00000493230.5:c.*59_*68del (HRAS) ENSP00000434023.1:n.*59_*68del
NM_001130442.1:c.490_499del (HRAS) NP_001123914.1:p.Arg164SerfsTer5
NM_005343.2:c.490_499del (HRAS) NP_005334.1:p.Arg164SerfsTer5
NM_176795.3:c.*59_*68del (HRAS) NP_789765.1:n.*59_*68del
XM_011519875.1:c.-425+4370_-425+4379del (LRRC56) XP_011518177.1:n.-425+4370_-425+4379del
XM_011519877.1:c.-162+4370_-162+4379del (LRRC56) XP_011518179.1:n.-162+4370_-162+4379del
XR_242795.1:n.771_780del (HRAS)
NM_001130442.2:c.490_499del (HRAS) NP_001123914.1:p.Arg164SerfsTer5
NM_001318054.1:c.253_262del (HRAS) NP_001304983.1:p.Arg85SerfsTer5
NM_005343.3:c.490_499del (HRAS) NP_005334.1:p.Arg164SerfsTer5
NM_176795.4:c.*59_*68del (HRAS) NP_789765.1:n.*59_*68del
XM_011519875.2:c.-425+4370_-425+4379del (LRRC56) XP_011518177.1:n.-425+4370_-425+4379del
XM_011519877.2:c.-162+4370_-162+4379del (LRRC56) XP_011518179.1:n.-162+4370_-162+4379del
XM_017017167.1:c.-500+4370_-500+4379del (LRRC56) XP_016872656.1:n.-500+4370_-500+4379del
XM_017017168.1:c.-500+4370_-500+4379del (LRRC56) XP_016872657.1:n.-500+4370_-500+4379del
NM_005343.4:c.490_499del (HRAS) MANE Select NP_005334.1:p.Arg164SerfsTer5
NM_001318054.2:c.253_262del (HRAS) NP_001304983.1:p.Arg85SerfsTer5
NM_001130442.3:c.490_499del (HRAS) NP_001123914.1:p.Arg164SerfsTer5
NM_176795.5:c.*59_*68del (HRAS) MANE Plus Clinical NP_789765.1:n.*59_*68del