Canonical Allele Identifier: CA1947153624

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.534049_534050delinsCT , CM000673.2:g.534049_534050delinsCT GRCh38
NC_000011.9:g.534049_534050delinsCT , CM000673.1:g.534049_534050delinsCT GRCh37
NC_000011.8:g.524049_524050delinsCT NCBI36
NG_007666.1:g.6501_6502delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.112-106_112-105delinsAG (HRAS) ENSP00000380722.3:n.112-106_112-105delinsAG
ENST00000417302.7:c.112-106_112-105delinsAG (HRAS) MANE Plus Clinical ENSP00000388246.1:n.112-106_112-105delinsAG
ENST00000417302.6:c.112-106_112-105delinsAG (HRAS) ENSP00000388246.1:n.112-106_112-105delinsAG
ENST00000462734.2:c.112-106_112-105delinsAG (HRAS) ENSP00000507303.1:n.112-106_112-105delinsAG
ENST00000311189.8:c.112-106_112-105delinsAG (HRAS) MANE Select ENSP00000309845.7:n.112-106_112-105delinsAG
ENST00000311189.7:c.112-106_112-105delinsAG (HRAS) ENSP00000309845.7:n.112-106_112-105delinsAG
ENST00000397594.5:c.112-106_112-105delinsAG (HRAS) ENSP00000380722.1:n.112-106_112-105delinsAG
ENST00000397596.6:c.112-106_112-105delinsAG (HRAS) ENSP00000380723.2:n.112-106_112-105delinsAG
ENST00000417302.5:c.112-106_112-105delinsAG (HRAS) ENSP00000388246.1:n.112-106_112-105delinsAG
ENST00000451590.5:c.112-106_112-105delinsAG (HRAS) ENSP00000407586.1:n.112-106_112-105delinsAG
ENST00000468682.2:n.600-106_600-105delinsAG (HRAS)
ENST00000493230.5:c.112-106_112-105delinsAG (HRAS) ENSP00000434023.1:n.112-106_112-105delinsAG
NM_001130442.1:c.112-106_112-105delinsAG (HRAS) NP_001123914.1:n.112-106_112-105delinsAG
NM_005343.2:c.112-106_112-105delinsAG (HRAS) NP_005334.1:n.112-106_112-105delinsAG
NM_176795.3:c.112-106_112-105delinsAG (HRAS) NP_789765.1:n.112-106_112-105delinsAG
XM_011519875.1:c.-424-4549_-424-4548delinsCT (LRRC56) XP_011518177.1:n.-424-4549_-424-4548delinsCT
XM_011519877.1:c.-161-5531_-161-5530delinsCT (LRRC56) XP_011518179.1:n.-161-5531_-161-5530delinsCT
XR_242795.1:n.311-106_311-105delinsAG (HRAS)
NM_001130442.2:c.112-106_112-105delinsAG (HRAS) NP_001123914.1:n.112-106_112-105delinsAG
NM_001318054.1:c.-208-106_-208-105delinsAG (HRAS) NP_001304983.1:n.-208-106_-208-105delinsAG
NM_005343.3:c.112-106_112-105delinsAG (HRAS) NP_005334.1:n.112-106_112-105delinsAG
NM_176795.4:c.112-106_112-105delinsAG (HRAS) NP_789765.1:n.112-106_112-105delinsAG
XM_011519875.2:c.-424-4549_-424-4548delinsCT (LRRC56) XP_011518177.1:n.-424-4549_-424-4548delinsCT
XM_011519877.2:c.-161-5531_-161-5530delinsCT (LRRC56) XP_011518179.1:n.-161-5531_-161-5530delinsCT
XM_017017167.1:c.-499-4474_-499-4473delinsCT (LRRC56) XP_016872656.1:n.-499-4474_-499-4473delinsCT
XM_017017168.1:c.-499-4474_-499-4473delinsCT (LRRC56) XP_016872657.1:n.-499-4474_-499-4473delinsCT
NM_005343.4:c.112-106_112-105delinsAG (HRAS) MANE Select NP_005334.1:n.112-106_112-105delinsAG
NM_001318054.2:c.-208-106_-208-105delinsAG (HRAS) NP_001304983.1:n.-208-106_-208-105delinsAG
NM_001130442.3:c.112-106_112-105delinsAG (HRAS) NP_001123914.1:n.112-106_112-105delinsAG
NM_176795.5:c.112-106_112-105delinsAG (HRAS) MANE Plus Clinical NP_789765.1:n.112-106_112-105delinsAG