Canonical Allele Identifier: CA2611691826

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.534101_534125del , CM000673.2:g.534101_534125del GRCh38
NC_000011.9:g.534101_534125del , CM000673.1:g.534101_534125del GRCh37
NC_000011.8:g.524101_524125del NCBI36
NG_007666.1:g.6429_6453del

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.111+90_111+114del (HRAS) ENSP00000380722.3:n.111+90_111+114del
ENST00000417302.7:c.111+90_111+114del (HRAS) MANE Plus Clinical ENSP00000388246.1:n.111+90_111+114del
ENST00000417302.6:c.111+90_111+114del (HRAS) ENSP00000388246.1:n.111+90_111+114del
ENST00000462734.2:c.111+90_111+114del (HRAS) ENSP00000507303.1:n.111+90_111+114del
ENST00000311189.8:c.111+90_111+114del (HRAS) MANE Select ENSP00000309845.7:n.111+90_111+114del
ENST00000311189.7:c.111+90_111+114del (HRAS) ENSP00000309845.7:n.111+90_111+114del
ENST00000397594.5:c.111+90_111+114del (HRAS) ENSP00000380722.1:n.111+90_111+114del
ENST00000397596.6:c.111+90_111+114del (HRAS) ENSP00000380723.2:n.111+90_111+114del
ENST00000417302.5:c.111+90_111+114del (HRAS) ENSP00000388246.1:n.111+90_111+114del
ENST00000451590.5:c.111+90_111+114del (HRAS) ENSP00000407586.1:n.111+90_111+114del
ENST00000468682.2:n.599+90_599+114del (HRAS)
ENST00000493230.5:c.111+90_111+114del (HRAS) ENSP00000434023.1:n.111+90_111+114del
NM_001130442.1:c.111+90_111+114del (HRAS) NP_001123914.1:n.111+90_111+114del
NM_005343.2:c.111+90_111+114del (HRAS) NP_005334.1:n.111+90_111+114del
NM_176795.3:c.111+90_111+114del (HRAS) NP_789765.1:n.111+90_111+114del
XM_011519875.1:c.-424-4497_-424-4473del (LRRC56) XP_011518177.1:n.-424-4497_-424-4473del
XM_011519877.1:c.-161-5479_-161-5455del (LRRC56) XP_011518179.1:n.-161-5479_-161-5455del
XR_242795.1:n.310+90_310+114del (HRAS)
NM_001130442.2:c.111+90_111+114del (HRAS) NP_001123914.1:n.111+90_111+114del
NM_001318054.1:c.-209+90_-209+114del (HRAS) NP_001304983.1:n.-209+90_-209+114del
NM_005343.3:c.111+90_111+114del (HRAS) NP_005334.1:n.111+90_111+114del
NM_176795.4:c.111+90_111+114del (HRAS) NP_789765.1:n.111+90_111+114del
XM_011519875.2:c.-424-4497_-424-4473del (LRRC56) XP_011518177.1:n.-424-4497_-424-4473del
XM_011519877.2:c.-161-5479_-161-5455del (LRRC56) XP_011518179.1:n.-161-5479_-161-5455del
XM_017017167.1:c.-499-4422_-499-4398del (LRRC56) XP_016872656.1:n.-499-4422_-499-4398del
XM_017017168.1:c.-499-4422_-499-4398del (LRRC56) XP_016872657.1:n.-499-4422_-499-4398del
NM_005343.4:c.111+90_111+114del (HRAS) MANE Select NP_005334.1:n.111+90_111+114del
NM_001318054.2:c.-209+90_-209+114del (HRAS) NP_001304983.1:n.-209+90_-209+114del
NM_001130442.3:c.111+90_111+114del (HRAS) NP_001123914.1:n.111+90_111+114del
NM_176795.5:c.111+90_111+114del (HRAS) MANE Plus Clinical NP_789765.1:n.111+90_111+114del