Canonical Allele Identifier: CA2611691604
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

gnomAD v4: 11-532504-TC-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532506del , CM000673.2:g.532506del GRCh38
NC_000011.9:g.532506del , CM000673.1:g.532506del GRCh37
NC_000011.8:g.522506del NCBI36
NG_007666.1:g.8046del

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*145del (HRAS) ENSP00000380722.3:n.*145del
ENST00000417302.7:c.*270del (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*270del
ENST00000397594.6:c.376del (HRAS) ENSP00000380722.2:n.376del
ENST00000417302.6:c.*270del (HRAS) ENSP00000388246.1:n.*270del
ENST00000462734.2:c.*205del (HRAS) ENSP00000507303.1:n.*205del
ENST00000311189.8:c.*23del (HRAS) MANE Select ENSP00000309845.7:n.*23del
ENST00000311189.7:c.*23del (HRAS) ENSP00000309845.7:n.*23del
ENST00000397594.5:c.*270del (HRAS) ENSP00000380722.1:n.*270del
ENST00000397596.6:c.*131del (HRAS) ENSP00000380723.2:n.*131del
ENST00000417302.5:c.*270del (HRAS) ENSP00000388246.1:n.*270del
ENST00000451590.5:c.*131del (HRAS) ENSP00000407586.1:n.*131del
ENST00000462734.1:n.368del (HRAS)
ENST00000478324.5:n.368del (HRAS)
ENST00000493230.5:c.*162del (HRAS) ENSP00000434023.1:n.*162del
NM_001130442.1:c.*131del (HRAS) NP_001123914.1:n.*131del
NM_005343.2:c.*23del (HRAS) NP_005334.1:n.*23del
NM_176795.3:c.*270del (HRAS) NP_789765.1:n.*270del
XM_011519875.1:c.-425+4169del (LRRC56) XP_011518177.1:n.-425+4169del
XM_011519877.1:c.-162+4169del (LRRC56) XP_011518179.1:n.-162+4169del
XR_242795.1:n.874del (HRAS)
NM_001130442.2:c.*131del (HRAS) NP_001123914.1:n.*131del
NM_001318054.1:c.*23del (HRAS) NP_001304983.1:n.*23del
NM_005343.3:c.*23del (HRAS) NP_005334.1:n.*23del
NM_176795.4:c.*270del (HRAS) NP_789765.1:n.*270del
XM_011519875.2:c.-425+4169del (LRRC56) XP_011518177.1:n.-425+4169del
XM_011519877.2:c.-162+4169del (LRRC56) XP_011518179.1:n.-162+4169del
XM_017017167.1:c.-500+4169del (LRRC56) XP_016872656.1:n.-500+4169del
XM_017017168.1:c.-500+4169del (LRRC56) XP_016872657.1:n.-500+4169del
NM_005343.4:c.*23del (HRAS) MANE Select NP_005334.1:n.*23del
NM_001318054.2:c.*23del (HRAS) NP_001304983.1:n.*23del
NM_001130442.3:c.*131del (HRAS) NP_001123914.1:n.*131del
NM_176795.5:c.*270del (HRAS) MANE Plus Clinical NP_789765.1:n.*270del
Search 100 bp 5'
Search 100 bp 3'