Canonical Allele Identifier: CA597019241

Linked Data

ClinVar Variation Id: 1400189
ClinVar RCV Id: RCV001918065
dbSNP Id: rs1564790048
MyVariant Identifiers: chr11:g.534207_534213del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.534209_534215del , CM000673.2:g.534209_534215del GRCh38
NC_000011.9:g.534209_534215del , CM000673.1:g.534209_534215del GRCh37
NC_000011.8:g.524209_524215del NCBI36
NG_007666.1:g.6338_6344del

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.110_111+5del (HRAS)
ENST00000417302.7:c.110_111+5del (HRAS)
ENST00000417302.6:c.110_111+5del (HRAS)
ENST00000462734.2:c.110_111+5del (HRAS)
ENST00000311189.8:c.110_111+5del (HRAS)
ENST00000311189.7:c.110_111+5del (HRAS)
ENST00000397594.5:c.110_111+5del (HRAS)
ENST00000397596.6:c.110_111+5del (HRAS)
ENST00000417302.5:c.110_111+5del (HRAS)
ENST00000451590.5:c.110_111+5del (HRAS)
ENST00000468682.2:n.598_599+5del (HRAS)
ENST00000493230.5:c.110_111+5del (HRAS)
NM_001130442.1:c.110_111+5del (HRAS)
NM_005343.2:c.110_111+5del (HRAS)
NM_176795.3:c.110_111+5del (HRAS)
XM_011519875.1:c.-424-4389_-424-4383del (LRRC56) XP_011518177.1:n.-424-4389_-424-4383del
XM_011519877.1:c.-161-5371_-161-5365del (LRRC56) XP_011518179.1:n.-161-5371_-161-5365del
XR_242795.1:n.309_310+5del (HRAS)
NM_001130442.2:c.110_111+5del (HRAS)
NM_001318054.1:c.-210_-209+5del (HRAS)
NM_005343.3:c.110_111+5del (HRAS)
NM_176795.4:c.110_111+5del (HRAS)
XM_011519875.2:c.-424-4389_-424-4383del (LRRC56) XP_011518177.1:n.-424-4389_-424-4383del
XM_011519877.2:c.-161-5371_-161-5365del (LRRC56) XP_011518179.1:n.-161-5371_-161-5365del
XM_017017167.1:c.-499-4314_-499-4308del (LRRC56) XP_016872656.1:n.-499-4314_-499-4308del
XM_017017168.1:c.-499-4314_-499-4308del (LRRC56) XP_016872657.1:n.-499-4314_-499-4308del
NM_005343.4:c.110_111+5del (HRAS)
NM_001318054.2:c.-210_-209+5del (HRAS)
NM_001130442.3:c.110_111+5del (HRAS)
NM_176795.5:c.110_111+5del (HRAS)