Canonical Allele Identifier: CA596781615
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

ClinVar Variation Id: 1609012
ClinVar RCV Id: RCV002149986
dbSNP Id: rs1159599721
gnomAD v2: 11-532762-A-AAGGAGGGATGGGATC
gnomAD v4: 11-532762-A-AAGGAGGGATGGGATC
MyVariant Identifiers: chr11:g.532762_532763insAGGAGGGATGGGATC (hg19) chr11:g.532762_532763insAGGAGGGATGGGATC (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532771_532785dup , CM000673.2:g.532771_532785dup GRCh38
NC_000011.9:g.532771_532785dup , CM000673.1:g.532771_532785dup GRCh37
NC_000011.8:g.522771_522785dup NCBI36
NG_007666.1:g.7774_7788dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*20-147_*20-133dup (HRAS) ENSP00000380722.3:n.*20-147_*20-133dup
ENST00000417302.7:c.*20-22_*20-8dup (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*20-22_*20-8dup
ENST00000397594.6:c.251-147_251-133dup (HRAS) ENSP00000380722.2:n.251-147_251-133dup
ENST00000417302.6:c.*20-22_*20-8dup (HRAS) ENSP00000388246.1:n.*20-22_*20-8dup
ENST00000462734.2:c.*63-22_*63-8dup (HRAS) ENSP00000507303.1:n.*63-22_*63-8dup
ENST00000311189.8:c.451-22_451-8dup (HRAS) MANE Select ENSP00000309845.7:n.451-22_451-8dup
ENST00000311189.7:c.451-22_451-8dup (HRAS) ENSP00000309845.7:n.451-22_451-8dup
ENST00000397594.5:c.*20-22_*20-8dup (HRAS) ENSP00000380722.1:n.*20-22_*20-8dup
ENST00000397596.6:c.451-22_451-8dup (HRAS) ENSP00000380723.2:n.451-22_451-8dup
ENST00000417302.5:c.*20-22_*20-8dup (HRAS) ENSP00000388246.1:n.*20-22_*20-8dup
ENST00000451590.5:c.451-22_451-8dup (HRAS) ENSP00000407586.1:n.451-22_451-8dup
ENST00000462734.1:n.226-22_226-8dup (HRAS)
ENST00000478324.5:n.243-147_243-133dup (HRAS)
ENST00000479482.1:n.372-22_372-8dup (HRAS)
ENST00000493230.5:c.*20-22_*20-8dup (HRAS) ENSP00000434023.1:n.*20-22_*20-8dup
NM_001130442.1:c.451-22_451-8dup (HRAS) NP_001123914.1:n.451-22_451-8dup
NM_005343.2:c.451-22_451-8dup (HRAS) NP_005334.1:n.451-22_451-8dup
NM_176795.3:c.*20-22_*20-8dup (HRAS) NP_789765.1:n.*20-22_*20-8dup
XM_011519875.1:c.-425+4434_-425+4448dup (LRRC56) XP_011518177.1:n.-425+4434_-425+4448dup
XM_011519877.1:c.-162+4434_-162+4448dup (LRRC56) XP_011518179.1:n.-162+4434_-162+4448dup
XR_242795.1:n.732-22_732-8dup (HRAS)
NM_001130442.2:c.451-22_451-8dup (HRAS) NP_001123914.1:n.451-22_451-8dup
NM_001318054.1:c.214-22_214-8dup (HRAS) NP_001304983.1:n.214-22_214-8dup
NM_005343.3:c.451-22_451-8dup (HRAS) NP_005334.1:n.451-22_451-8dup
NM_176795.4:c.*20-22_*20-8dup (HRAS) NP_789765.1:n.*20-22_*20-8dup
XM_011519875.2:c.-425+4434_-425+4448dup (LRRC56) XP_011518177.1:n.-425+4434_-425+4448dup
XM_011519877.2:c.-162+4434_-162+4448dup (LRRC56) XP_011518179.1:n.-162+4434_-162+4448dup
XM_017017167.1:c.-500+4434_-500+4448dup (LRRC56) XP_016872656.1:n.-500+4434_-500+4448dup
XM_017017168.1:c.-500+4434_-500+4448dup (LRRC56) XP_016872657.1:n.-500+4434_-500+4448dup
NM_005343.4:c.451-22_451-8dup (HRAS) MANE Select NP_005334.1:n.451-22_451-8dup
NM_001318054.2:c.214-22_214-8dup (HRAS) NP_001304983.1:n.214-22_214-8dup
NM_001130442.3:c.451-22_451-8dup (HRAS) NP_001123914.1:n.451-22_451-8dup
NM_176795.5:c.*20-22_*20-8dup (HRAS) MANE Plus Clinical NP_789765.1:n.*20-22_*20-8dup
Search 100 bp 5'
Search 100 bp 3'