Canonical Allele Identifier: CA378921140
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

ClinVar Variation Id: 1408362
ClinVar RCV Id: RCV001938019
dbSNP Id: rs1439562437
gnomAD v3: 11-532710-G-A
gnomAD v4: 11-532710-G-A
MyVariant Identifiers: chr11:g.532710G>A (hg19) chr11:g.532710G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532710G>A , CM000673.2:g.532710G>A GRCh38
NC_000011.9:g.532710G>A , CM000673.1:g.532710G>A GRCh37
NC_000011.8:g.522710G>A NCBI36
NG_007666.1:g.7841C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*20-80C>T (HRAS) ENSP00000380722.3:n.*20-80C>T
ENST00000417302.7:c.*65C>T (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*65C>T
ENST00000397594.6:c.251-80C>T (HRAS) ENSP00000380722.2:n.251-80C>T
ENST00000417302.6:c.*65C>T (HRAS) ENSP00000388246.1:n.*65C>T
ENST00000462734.2:c.*108C>T (HRAS) ENSP00000507303.1:n.*108C>T
ENST00000311189.8:c.496C>T (HRAS) MANE Select ENSP00000309845.7:p.His166Tyr
ENST00000311189.7:c.496C>T (HRAS) ENSP00000309845.7:p.His166Tyr
ENST00000397594.5:c.*65C>T (HRAS) ENSP00000380722.1:n.*65C>T
ENST00000397596.6:c.496C>T (HRAS) ENSP00000380723.2:p.His166Tyr
ENST00000417302.5:c.*65C>T (HRAS) ENSP00000388246.1:n.*65C>T
ENST00000451590.5:c.496C>T (HRAS) ENSP00000407586.1:p.His166Tyr
ENST00000462734.1:n.271C>T (HRAS)
ENST00000478324.5:n.243-80C>T (HRAS)
ENST00000479482.1:n.417C>T (HRAS)
ENST00000493230.5:c.*65C>T (HRAS) ENSP00000434023.1:n.*65C>T
NM_001130442.1:c.496C>T (HRAS) NP_001123914.1:p.His166Tyr
NM_005343.2:c.496C>T (HRAS) NP_005334.1:p.His166Tyr
NM_176795.3:c.*65C>T (HRAS) NP_789765.1:n.*65C>T
XM_011519875.1:c.-425+4373G>A (LRRC56) XP_011518177.1:n.-425+4373G>A
XM_011519877.1:c.-162+4373G>A (LRRC56) XP_011518179.1:n.-162+4373G>A
XR_242795.1:n.777C>T (HRAS)
NM_001130442.2:c.496C>T (HRAS) NP_001123914.1:p.His166Tyr
NM_001318054.1:c.259C>T (HRAS) NP_001304983.1:p.His87Tyr
NM_005343.3:c.496C>T (HRAS) NP_005334.1:p.His166Tyr
NM_176795.4:c.*65C>T (HRAS) NP_789765.1:n.*65C>T
XM_011519875.2:c.-425+4373G>A (LRRC56) XP_011518177.1:n.-425+4373G>A
XM_011519877.2:c.-162+4373G>A (LRRC56) XP_011518179.1:n.-162+4373G>A
XM_017017167.1:c.-500+4373G>A (LRRC56) XP_016872656.1:n.-500+4373G>A
XM_017017168.1:c.-500+4373G>A (LRRC56) XP_016872657.1:n.-500+4373G>A
NM_005343.4:c.496C>T (HRAS) MANE Select NP_005334.1:p.His166Tyr
NM_001318054.2:c.259C>T (HRAS) NP_001304983.1:p.His87Tyr
NM_001130442.3:c.496C>T (HRAS) NP_001123914.1:p.His166Tyr
NM_176795.5:c.*65C>T (HRAS) MANE Plus Clinical NP_789765.1:n.*65C>T
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