Canonical Allele Identifier: CA596781455
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

dbSNP Id: rs1463252537
gnomAD v2: 11-532358-C-CG
gnomAD v3: 11-532358-C-CG
gnomAD v4: 11-532358-C-CG
MyVariant Identifiers: chr11:g.532358_532359insG (hg19) chr11:g.532358_532359insG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532358_532359insG , CM000673.2:g.532358_532359insG GRCh38
NC_000011.9:g.532358_532359insG , CM000673.1:g.532358_532359insG GRCh37
NC_000011.8:g.522358_522359insG NCBI36
NG_007666.1:g.8192_8193insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*291_*292insC (HRAS) ENSP00000380722.3:n.*291_*292insC
ENST00000417302.7:c.*416_*417insC (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*416_*417insC
ENST00000397594.6:c.522_523insC (HRAS) ENSP00000380722.2:n.522_523insC
ENST00000417302.6:c.*416_*417insC (HRAS) ENSP00000388246.1:n.*416_*417insC
ENST00000462734.2:c.*351_*352insC (HRAS) ENSP00000507303.1:n.*351_*352insC
ENST00000311189.8:c.*169_*170insC (HRAS) MANE Select ENSP00000309845.7:n.*169_*170insC
ENST00000397594.5:c.*416_*417insC (HRAS) ENSP00000380722.1:n.*416_*417insC
ENST00000397596.6:c.*277_*278insC (HRAS) ENSP00000380723.2:n.*277_*278insC
ENST00000417302.5:c.*416_*417insC (HRAS) ENSP00000388246.1:n.*416_*417insC
ENST00000451590.5:c.*277_*278insC (HRAS) ENSP00000407586.1:n.*277_*278insC
ENST00000462734.1:n.514_515insC (HRAS)
ENST00000478324.5:n.514_515insC (HRAS)
ENST00000493230.5:c.*308_*309insC (HRAS) ENSP00000434023.1:n.*308_*309insC
NM_001130442.1:c.*277_*278insC (HRAS) NP_001123914.1:n.*277_*278insC
NM_005343.2:c.*169_*170insC (HRAS) NP_005334.1:n.*169_*170insC
NM_176795.3:c.*416_*417insC (HRAS) NP_789765.1:n.*416_*417insC
XM_011519875.1:c.-425+4021_-425+4022insG (LRRC56) XP_011518177.1:n.-425+4021_-425+4022insG
XM_011519877.1:c.-162+4021_-162+4022insG (LRRC56) XP_011518179.1:n.-162+4021_-162+4022insG
XR_242795.1:n.1020_1021insC (HRAS)
NM_001130442.2:c.*277_*278insC (HRAS) NP_001123914.1:n.*277_*278insC
NM_001318054.1:c.*169_*170insC (HRAS) NP_001304983.1:n.*169_*170insC
NM_005343.3:c.*169_*170insC (HRAS) NP_005334.1:n.*169_*170insC
NM_176795.4:c.*416_*417insC (HRAS) NP_789765.1:n.*416_*417insC
XM_011519875.2:c.-425+4021_-425+4022insG (LRRC56) XP_011518177.1:n.-425+4021_-425+4022insG
XM_011519877.2:c.-162+4021_-162+4022insG (LRRC56) XP_011518179.1:n.-162+4021_-162+4022insG
XM_017017167.1:c.-500+4021_-500+4022insG (LRRC56) XP_016872656.1:n.-500+4021_-500+4022insG
XM_017017168.1:c.-500+4021_-500+4022insG (LRRC56) XP_016872657.1:n.-500+4021_-500+4022insG
NM_005343.4:c.*169_*170insC (HRAS) MANE Select NP_005334.1:n.*169_*170insC
NM_001318054.2:c.*169_*170insC (HRAS) NP_001304983.1:n.*169_*170insC
NM_001130442.3:c.*277_*278insC (HRAS) NP_001123914.1:n.*277_*278insC
NM_176795.5:c.*416_*417insC (HRAS) MANE Plus Clinical NP_789765.1:n.*416_*417insC
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