Canonical Allele Identifier: CA677772761
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

dbSNP Id: rs1258580925
gnomAD v3: 11-532504-T-TC
gnomAD v4: 11-532504-T-TC
MyVariant Identifiers: chr11:g.532504_532505insC (hg19) chr11:g.532504_532505insC (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

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