Canonical Allele Identifier: CA1947140498

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532430_532454delinsCCCTTCCTTCCTTCCTTGCTTCCGT , CM000673.2:g.532430_532454delinsCCCTTCCTTCCTTCCTTGCTTCCGT GRCh38
NC_000011.9:g.532430_532454delinsCCCTTCCTTCCTTCCTTGCTTCCGT , CM000673.1:g.532430_532454delinsCCCTTCCTTCCTTCCTTGCTTCCGT GRCh37
NC_000011.8:g.522430_522454delinsCCCTTCCTTCCTTCCTTGCTTCCGT NCBI36
NG_007666.1:g.8097_8121delinsACGGAAGCAAGGAAGGAAGGAAGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*196_*220delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) ENSP00000380722.3:n.*196_*220delinsACGGAAGCAAGGAAGGAAGGAAGGG
ENST00000417302.7:c.*321_*345delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*321_*345delinsACGGAAGCAAGGAAGGAAGGAAGGG
ENST00000397594.6:c.427_451delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) ENSP00000380722.2:n.427_451delinsACGGAAGCAAGGAAGGAAGGAAGGG
ENST00000417302.6:c.*321_*345delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) ENSP00000388246.1:n.*321_*345delinsACGGAAGCAAGGAAGGAAGGAAGGG
ENST00000462734.2:c.*256_*280delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) ENSP00000507303.1:n.*256_*280delinsACGGAAGCAAGGAAGGAAGGAAGGG
ENST00000311189.8:c.*74_*98delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) MANE Select ENSP00000309845.7:n.*74_*98delinsACGGAAGCAAGGAAGGAAGGAAGGG
ENST00000311189.7:c.*74_*98delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) ENSP00000309845.7:n.*74_*98delinsACGGAAGCAAGGAAGGAAGGAAGGG
ENST00000397594.5:c.*321_*345delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) ENSP00000380722.1:n.*321_*345delinsACGGAAGCAAGGAAGGAAGGAAGGG
ENST00000397596.6:c.*182_*206delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) ENSP00000380723.2:n.*182_*206delinsACGGAAGCAAGGAAGGAAGGAAGGG
ENST00000417302.5:c.*321_*345delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) ENSP00000388246.1:n.*321_*345delinsACGGAAGCAAGGAAGGAAGGAAGGG
ENST00000451590.5:c.*182_*206delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) ENSP00000407586.1:n.*182_*206delinsACGGAAGCAAGGAAGGAAGGAAGGG
ENST00000462734.1:n.419_443delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS)
ENST00000478324.5:n.419_443delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS)
ENST00000493230.5:c.*213_*237delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) ENSP00000434023.1:n.*213_*237delinsACGGAAGCAAGGAAGGAAGGAAGGG
NM_001130442.1:c.*182_*206delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) NP_001123914.1:n.*182_*206delinsACGGAAGCAAGGAAGGAAGGAAGGG
NM_005343.2:c.*74_*98delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) NP_005334.1:n.*74_*98delinsACGGAAGCAAGGAAGGAAGGAAGGG
NM_176795.3:c.*321_*345delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) NP_789765.1:n.*321_*345delinsACGGAAGCAAGGAAGGAAGGAAGGG
XM_011519875.1:c.-425+4093_-425+4117delinsCCCTTCCTTCCTTCCTTGCTTCCGT (LRRC56) XP_011518177.1:n.-425+4093_-425+4117delinsCCCTTCCTTCCTTCCTTGC...
XM_011519877.1:c.-162+4093_-162+4117delinsCCCTTCCTTCCTTCCTTGCTTCCGT (LRRC56) XP_011518179.1:n.-162+4093_-162+4117delinsCCCTTCCTTCCTTCCTTGC...
XR_242795.1:n.925_949delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS)
NM_001130442.2:c.*182_*206delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) NP_001123914.1:n.*182_*206delinsACGGAAGCAAGGAAGGAAGGAAGGG
NM_001318054.1:c.*74_*98delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) NP_001304983.1:n.*74_*98delinsACGGAAGCAAGGAAGGAAGGAAGGG
NM_005343.3:c.*74_*98delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) NP_005334.1:n.*74_*98delinsACGGAAGCAAGGAAGGAAGGAAGGG
NM_176795.4:c.*321_*345delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) NP_789765.1:n.*321_*345delinsACGGAAGCAAGGAAGGAAGGAAGGG
XM_011519875.2:c.-425+4093_-425+4117delinsCCCTTCCTTCCTTCCTTGCTTCCGT (LRRC56) XP_011518177.1:n.-425+4093_-425+4117delinsCCCTTCCTTCCTTCCTTGC...
XM_011519877.2:c.-162+4093_-162+4117delinsCCCTTCCTTCCTTCCTTGCTTCCGT (LRRC56) XP_011518179.1:n.-162+4093_-162+4117delinsCCCTTCCTTCCTTCCTTGC...
XM_017017167.1:c.-500+4093_-500+4117delinsCCCTTCCTTCCTTCCTTGCTTCCGT (LRRC56) XP_016872656.1:n.-500+4093_-500+4117delinsCCCTTCCTTCCTTCCTTGC...
XM_017017168.1:c.-500+4093_-500+4117delinsCCCTTCCTTCCTTCCTTGCTTCCGT (LRRC56) XP_016872657.1:n.-500+4093_-500+4117delinsCCCTTCCTTCCTTCCTTGC...
NM_005343.4:c.*74_*98delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) MANE Select NP_005334.1:n.*74_*98delinsACGGAAGCAAGGAAGGAAGGAAGGG
NM_001318054.2:c.*74_*98delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) NP_001304983.1:n.*74_*98delinsACGGAAGCAAGGAAGGAAGGAAGGG
NM_001130442.3:c.*182_*206delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) NP_001123914.1:n.*182_*206delinsACGGAAGCAAGGAAGGAAGGAAGGG
NM_176795.5:c.*321_*345delinsACGGAAGCAAGGAAGGAAGGAAGGG (HRAS) MANE Plus Clinical NP_789765.1:n.*321_*345delinsACGGAAGCAAGGAAGGAAGGAAGGG