Canonical Allele Identifier: CA2611691743
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

gnomAD v4: 11-532603-T-TGGCGGCCGC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532604_532612dup , CM000673.2:g.532604_532612dup GRCh38
NC_000011.9:g.532604_532612dup , CM000673.1:g.532604_532612dup GRCh37
NC_000011.8:g.522604_522612dup NCBI36
NG_007666.1:g.7939_7947dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*38_*46dup (HRAS) ENSP00000380722.3:n.*38_*46dup
ENST00000417302.7:c.*163_*171dup (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*163_*171dup
ENST00000397594.6:c.269_277dup (HRAS) ENSP00000380722.2:n.269_277dup
ENST00000417302.6:c.*163_*171dup (HRAS) ENSP00000388246.1:n.*163_*171dup
ENST00000462734.2:c.*187+19_*187+27dup (HRAS) ENSP00000507303.1:n.*187+19_*187+27dup
ENST00000311189.8:c.*5+19_*5+27dup (HRAS) MANE Select ENSP00000309845.7:n.*5+19_*5+27dup
ENST00000311189.7:c.*5+19_*5+27dup (HRAS) ENSP00000309845.7:n.*5+19_*5+27dup
ENST00000397594.5:c.*163_*171dup (HRAS) ENSP00000380722.1:n.*163_*171dup
ENST00000397596.6:c.*24_*32dup (HRAS) ENSP00000380723.2:n.*24_*32dup
ENST00000417302.5:c.*163_*171dup (HRAS) ENSP00000388246.1:n.*163_*171dup
ENST00000451590.5:c.*24_*32dup (HRAS) ENSP00000407586.1:n.*24_*32dup
ENST00000462734.1:n.350+19_350+27dup (HRAS)
ENST00000478324.5:n.261_269dup (HRAS)
ENST00000493230.5:c.*144+19_*144+27dup (HRAS) ENSP00000434023.1:n.*144+19_*144+27dup
NM_001130442.1:c.*24_*32dup (HRAS) NP_001123914.1:n.*24_*32dup
NM_005343.2:c.*5+19_*5+27dup (HRAS) NP_005334.1:n.*5+19_*5+27dup
NM_176795.3:c.*163_*171dup (HRAS) NP_789765.1:n.*163_*171dup
XM_011519875.1:c.-425+4267_-425+4275dup (LRRC56) XP_011518177.1:n.-425+4267_-425+4275dup
XM_011519877.1:c.-162+4267_-162+4275dup (LRRC56) XP_011518179.1:n.-162+4267_-162+4275dup
XR_242795.1:n.856+19_856+27dup (HRAS)
NM_001130442.2:c.*24_*32dup (HRAS) NP_001123914.1:n.*24_*32dup
NM_001318054.1:c.*5+19_*5+27dup (HRAS) NP_001304983.1:n.*5+19_*5+27dup
NM_005343.3:c.*5+19_*5+27dup (HRAS) NP_005334.1:n.*5+19_*5+27dup
NM_176795.4:c.*163_*171dup (HRAS) NP_789765.1:n.*163_*171dup
XM_011519875.2:c.-425+4267_-425+4275dup (LRRC56) XP_011518177.1:n.-425+4267_-425+4275dup
XM_011519877.2:c.-162+4267_-162+4275dup (LRRC56) XP_011518179.1:n.-162+4267_-162+4275dup
XM_017017167.1:c.-500+4267_-500+4275dup (LRRC56) XP_016872656.1:n.-500+4267_-500+4275dup
XM_017017168.1:c.-500+4267_-500+4275dup (LRRC56) XP_016872657.1:n.-500+4267_-500+4275dup
NM_005343.4:c.*5+19_*5+27dup (HRAS) MANE Select NP_005334.1:n.*5+19_*5+27dup
NM_001318054.2:c.*5+19_*5+27dup (HRAS) NP_001304983.1:n.*5+19_*5+27dup
NM_001130442.3:c.*24_*32dup (HRAS) NP_001123914.1:n.*24_*32dup
NM_176795.5:c.*163_*171dup (HRAS) MANE Plus Clinical NP_789765.1:n.*163_*171dup
Search 100 bp 5'
Search 100 bp 3'