Canonical Allele Identifier: CA2611691411
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

gnomAD v4: 11-533833-C-CGGT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.533835_533837dup , CM000673.2:g.533835_533837dup GRCh38
NC_000011.9:g.533835_533837dup , CM000673.1:g.533835_533837dup GRCh37
NC_000011.8:g.523835_523837dup NCBI36
NG_007666.1:g.6715_6717dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.220_222dup (HRAS) ENSP00000380722.3:p.Thr74_Gly75insThr
ENST00000417302.7:c.220_222dup (HRAS) MANE Plus Clinical ENSP00000388246.1:p.Thr74_Gly75insThr
ENST00000417302.6:c.220_222dup (HRAS) ENSP00000388246.1:p.Thr74_Gly75insThr
ENST00000462734.2:c.220_222dup (HRAS) ENSP00000507303.1:p.Thr74_Gly75insThr
ENST00000311189.8:c.220_222dup (HRAS) MANE Select ENSP00000309845.7:p.Thr74_Gly75insThr
ENST00000311189.7:c.220_222dup (HRAS) ENSP00000309845.7:p.Thr74_Gly75insThr
ENST00000397594.5:c.220_222dup (HRAS) ENSP00000380722.1:p.Thr74_Gly75insThr
ENST00000397596.6:c.220_222dup (HRAS) ENSP00000380723.2:p.Thr74_Gly75insThr
ENST00000417302.5:c.220_222dup (HRAS) ENSP00000388246.1:p.Thr74_Gly75insThr
ENST00000451590.5:c.220_222dup (HRAS) ENSP00000407586.1:p.Thr74_Gly75insThr
ENST00000468682.2:n.708_710dup (HRAS)
ENST00000479482.1:n.141_143dup (HRAS)
ENST00000493230.5:c.220_222dup (HRAS) ENSP00000434023.1:p.Thr74_Gly75insThr
NM_001130442.1:c.220_222dup (HRAS) NP_001123914.1:p.Thr74_Gly75insThr
NM_005343.2:c.220_222dup (HRAS) NP_005334.1:p.Thr74_Gly75insThr
NM_176795.3:c.220_222dup (HRAS) NP_789765.1:p.Thr74_Gly75insThr
XM_011519875.1:c.-424-4763_-424-4761dup (LRRC56) XP_011518177.1:n.-424-4763_-424-4761dup
XM_011519877.1:c.-162+5498_-162+5500dup (LRRC56) XP_011518179.1:n.-162+5498_-162+5500dup
XR_242795.1:n.419_421dup (HRAS)
NM_001130442.2:c.220_222dup (HRAS) NP_001123914.1:p.Thr74_Gly75insThr
NM_001318054.1:c.-100_-98dup (HRAS) NP_001304983.1:n.-100_-98dup
NM_005343.3:c.220_222dup (HRAS) NP_005334.1:p.Thr74_Gly75insThr
NM_176795.4:c.220_222dup (HRAS) NP_789765.1:p.Thr74_Gly75insThr
XM_011519875.2:c.-424-4763_-424-4761dup (LRRC56) XP_011518177.1:n.-424-4763_-424-4761dup
XM_011519877.2:c.-162+5498_-162+5500dup (LRRC56) XP_011518179.1:n.-162+5498_-162+5500dup
XM_017017167.1:c.-499-4688_-499-4686dup (LRRC56) XP_016872656.1:n.-499-4688_-499-4686dup
XM_017017168.1:c.-499-4688_-499-4686dup (LRRC56) XP_016872657.1:n.-499-4688_-499-4686dup
NM_005343.4:c.220_222dup (HRAS) MANE Select NP_005334.1:p.Thr74_Gly75insThr
NM_001318054.2:c.-100_-98dup (HRAS) NP_001304983.1:n.-100_-98dup
NM_001130442.3:c.220_222dup (HRAS) NP_001123914.1:p.Thr74_Gly75insThr
NM_176795.5:c.220_222dup (HRAS) MANE Plus Clinical NP_789765.1:p.Thr74_Gly75insThr
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