Canonical Allele Identifier: CA1947140559
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532453_532457delinsGTCCT , CM000673.2:g.532453_532457delinsGTCCT GRCh38
NC_000011.9:g.532453_532457delinsGTCCT , CM000673.1:g.532453_532457delinsGTCCT GRCh37
NC_000011.8:g.522453_522457delinsGTCCT NCBI36
NG_007666.1:g.8094_8098delinsAGGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*193_*197delinsAGGAC (HRAS) ENSP00000380722.3:n.*193_*197delinsAGGAC
ENST00000417302.7:c.*318_*322delinsAGGAC (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*318_*322delinsAGGAC
ENST00000397594.6:c.424_428delinsAGGAC (HRAS) ENSP00000380722.2:n.424_428delinsAGGAC
ENST00000417302.6:c.*318_*322delinsAGGAC (HRAS) ENSP00000388246.1:n.*318_*322delinsAGGAC
ENST00000462734.2:c.*253_*257delinsAGGAC (HRAS) ENSP00000507303.1:n.*253_*257delinsAGGAC
ENST00000311189.8:c.*71_*75delinsAGGAC (HRAS) MANE Select ENSP00000309845.7:n.*71_*75delinsAGGAC
ENST00000311189.7:c.*71_*75delinsAGGAC (HRAS) ENSP00000309845.7:n.*71_*75delinsAGGAC
ENST00000397594.5:c.*318_*322delinsAGGAC (HRAS) ENSP00000380722.1:n.*318_*322delinsAGGAC
ENST00000397596.6:c.*179_*183delinsAGGAC (HRAS) ENSP00000380723.2:n.*179_*183delinsAGGAC
ENST00000417302.5:c.*318_*322delinsAGGAC (HRAS) ENSP00000388246.1:n.*318_*322delinsAGGAC
ENST00000451590.5:c.*179_*183delinsAGGAC (HRAS) ENSP00000407586.1:n.*179_*183delinsAGGAC
ENST00000462734.1:n.416_420delinsAGGAC (HRAS)
ENST00000478324.5:n.416_420delinsAGGAC (HRAS)
ENST00000493230.5:c.*210_*214delinsAGGAC (HRAS) ENSP00000434023.1:n.*210_*214delinsAGGAC
NM_001130442.1:c.*179_*183delinsAGGAC (HRAS) NP_001123914.1:n.*179_*183delinsAGGAC
NM_005343.2:c.*71_*75delinsAGGAC (HRAS) NP_005334.1:n.*71_*75delinsAGGAC
NM_176795.3:c.*318_*322delinsAGGAC (HRAS) NP_789765.1:n.*318_*322delinsAGGAC
XM_011519875.1:c.-425+4116_-425+4120delinsGTCCT (LRRC56) XP_011518177.1:n.-425+4116_-425+4120delinsGTCCT
XM_011519877.1:c.-162+4116_-162+4120delinsGTCCT (LRRC56) XP_011518179.1:n.-162+4116_-162+4120delinsGTCCT
XR_242795.1:n.922_926delinsAGGAC (HRAS)
NM_001130442.2:c.*179_*183delinsAGGAC (HRAS) NP_001123914.1:n.*179_*183delinsAGGAC
NM_001318054.1:c.*71_*75delinsAGGAC (HRAS) NP_001304983.1:n.*71_*75delinsAGGAC
NM_005343.3:c.*71_*75delinsAGGAC (HRAS) NP_005334.1:n.*71_*75delinsAGGAC
NM_176795.4:c.*318_*322delinsAGGAC (HRAS) NP_789765.1:n.*318_*322delinsAGGAC
XM_011519875.2:c.-425+4116_-425+4120delinsGTCCT (LRRC56) XP_011518177.1:n.-425+4116_-425+4120delinsGTCCT
XM_011519877.2:c.-162+4116_-162+4120delinsGTCCT (LRRC56) XP_011518179.1:n.-162+4116_-162+4120delinsGTCCT
XM_017017167.1:c.-500+4116_-500+4120delinsGTCCT (LRRC56) XP_016872656.1:n.-500+4116_-500+4120delinsGTCCT
XM_017017168.1:c.-500+4116_-500+4120delinsGTCCT (LRRC56) XP_016872657.1:n.-500+4116_-500+4120delinsGTCCT
NM_005343.4:c.*71_*75delinsAGGAC (HRAS) MANE Select NP_005334.1:n.*71_*75delinsAGGAC
NM_001318054.2:c.*71_*75delinsAGGAC (HRAS) NP_001304983.1:n.*71_*75delinsAGGAC
NM_001130442.3:c.*179_*183delinsAGGAC (HRAS) NP_001123914.1:n.*179_*183delinsAGGAC
NM_176795.5:c.*318_*322delinsAGGAC (HRAS) MANE Plus Clinical NP_789765.1:n.*318_*322delinsAGGAC
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