accessibility menu, dialog, popup

UserName
Viewing profile as user:

Please enter the information below and press OK to send your cart to Core Services for purchase.

    

System Message

OKCancel
LOADING ...
See other HRAS CNV Assays ›
Gene Symbol
HRAS
Assay Reference Genome
Location

Chr.11:533782 on build GRCh38
Cytoband
11p15.5
Assay ID Hs00134726_cn
Size
Availability Made To Order
Catalog # 4400291
Price
Your Price
Online offer:
Check your price ›

Assay Details

Target Gene Details

Entrez Gene ID:

 3265

Gene Name:

 HRas proto-oncogene, GTPase

Gene Aliases:

 C-BAS/HAS, C-H-RAS, C-HA-RAS1, CTLO, H-RASIDX, HAMSV, HRAS1, RASH1, p21ras

Location:

 Chr.11:532242-535567 on Build GRCh38

Assay Gene Location:

 Overlaps Intron 3 - Exon 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
HRAS NM_001130442.2 NP_001123914.1
NM_001318054.1 NP_001304983.1
NM_005343.3 NP_005334.1
NM_176795.4 NP_789765.1
AB451336.1
AB451485.1
AF493916.1 AAM12630.1
AJ437024.1 CAD24594.1
BC006499.2 AAH06499.1
BC095471.1 AAH95471.1
BM801600.1
BM801632.1
BQ674260.1
BT019421.1 AAV38228.1
CR536579.1 CAG38816.1
CR542271.1 CAG47067.1
KJ534867.1
KJ534868.1

Target Gene Details

Entrez Gene ID:

 115399

Gene Name:

 leucine rich repeat containing 56

Gene Aliases:

 -

Location:

 Chr.11:518967-554916 on Build GRCh38

Assay Gene Location:

 Within Intron 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
LRRC56 XM_011519875.2 XP_011518177.1
XM_011519877.2 XP_011518179.1
XM_017017167.1 XP_016872656.1
XM_017017168.1 XP_016872657.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv552854 Chr.11:511805 - 619789 on Build GRCh38 Loss MIR210HG LMNTD2 LOC143666 RASSF7 LRRC56 LOC101059906 PHRF1 HRAS IRF7 CDHR5 MIR210
nsv527327 Chr.11:295343 - 620599 on Build GRCh38 Loss RNH1 PKP3 B4GALNT4 LOC143666 IFITM2 PTDSS2 HRAS IRF7 CDHR5 IFITM5 MIR210 IFITM1 MIR210HG SIGIRR PGGHG LMNTD2 RASSF7 LRRC56 IFITM3 LOC101059906 PHRF1 ANO9
nsv951270 Chr.11:528401 - 628100 on Build GRCh38 Deletion MIR210HG SCT LMNTD2 LOC143666 RASSF7 LRRC56 LOC101059906 PHRF1 HRAS IRF7 CDHR5 MIR210
nsv469923 Chr.11:378188 - 1302334 on Build GRCh38 Loss PIDD1 RPLP2 TMEM80 RNH1 SCT MUC2 POLR2L PKP3 LOC143666 DRD4 MIR6744 MUC6 PNPLA2 MUC5B PTDSS2 HRAS CD151 MIR210 MIR210HG SLC25A22 EPS8L2 RASSF7 LRRC56 TSPAN4 LOC101059906 LOC101927503 ANO9 CEND1 B4GALNT4 AP2A2 CRACR2B MUC5AC IRF7 CDHR5 TALDO1 CHID1 SIGIRR PANO1 LMNTD2 TOLLIP PDDC1 LOC171391 SNORA52 PHRF1 DEAF1
esv2759794 Chr.11:409846 - 1336162 on Build GRCh38 Loss PIDD1 RPLP2 TMEM80 RNH1 SCT MUC2 POLR2L LOC143666 DRD4 MIR6744 MUC6 PNPLA2 MUC5B PTDSS2 HRAS CD151 MIR210 MIR210HG SLC25A22 EPS8L2 RASSF7 LRRC56 TSPAN4 LOC101059906 LOC101927503 ANO9 CEND1 TOLLIP-AS1 AP2A2 CRACR2B MUC5AC IRF7 CDHR5 TALDO1 CHID1 SIGIRR PANO1 LMNTD2 TOLLIP PDDC1 LOC171391 SNORA52 PHRF1 DEAF1
dgv182e199 Chr.11:349830 - 943372 on Build GRCh38 Deletion PIDD1 RPLP2 TMEM80 RNH1 SCT POLR2L PKP3 LOC143666 DRD4 PNPLA2 PTDSS2 HRAS CD151 MIR210 MIR210HG SLC25A22 EPS8L2 RASSF7 LRRC56 TSPAN4 LOC101059906 ANO9 CEND1 B4GALNT4 AP2A2 CRACR2B IRF7 CDHR5 TALDO1 CHID1 SIGIRR PANO1 LMNTD2 PDDC1 LOC171391 SNORA52 PHRF1 DEAF1
nsv1053964 Chr.11:491334 - 692433 on Build GRCh38 Gain RNH1 SCT LOC143666 DRD4 PTDSS2 HRAS IRF7 CDHR5 MIR210 MIR210HG LMNTD2 RASSF7 LRRC56 LOC101059906 PHRF1 DEAF1
nsv1159791 Chr.11:461793 - 909492 on Build GRCh38 Deletion PIDD1 RPLP2 TMEM80 RNH1 SCT POLR2L LOC143666 DRD4 PNPLA2 PTDSS2 HRAS CD151 MIR210 MIR210HG SLC25A22 EPS8L2 RASSF7 LRRC56 TSPAN4 LOC101059906 CEND1 CRACR2B IRF7 CDHR5 TALDO1 CHID1 PANO1 LMNTD2 PDDC1 LOC171391 SNORA52 PHRF1 DEAF1
nsv552855 Chr.11:532923 - 545087 on Build GRCh38 Loss LRRC56 HRAS

Back To Top

More Information


Set Membership:

 Intragenic Intronic Non-exonic DGV Variation

Panther Classification:

Molecular Function -

small GTPase

Gene Ontology Categories:

Function(s) Process(es)


Back To Top

Related Products