Genomic Map
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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: | Within Exon 4 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| HRAS | NM_001130442.2 | 4 | 572 | NP_001123914.1 |
| NM_001318054.1 | 4 | 572 | NP_001304983.1 | |
| NM_005343.3 | 4 | 572 | NP_005334.1 | |
| NM_176795.4 | 4 | 572 | NP_789765.1 | |
| AB451336.1 | 3 | 367 | ||
| AB451485.1 | 3 | 367 | ||
| AF493916.1 | 3 | 367 | AAM12630.1 | |
| AJ437024.1 | 3 | 367 | CAD24594.1 | |
| BC006499.2 | 4 | 543 | AAH06499.1 | |
| BC095471.1 | 3 | 368 | AAH95471.1 | |
| BM801600.1 | 4 | 495 | ||
| BM801632.1 | 4 | 555 | ||
| BQ674260.1 | 3 | 430 | ||
| BT019421.1 | 3 | 367 | AAV38228.1 | |
| CR536579.1 | 3 | 367 | CAG38816.1 | |
| CR542271.1 | 3 | 367 | CAG47067.1 | |
| KJ534867.1 | 3 | 367 | ||
| KJ534868.1 | 3 | 367 |
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 |
|---|---|---|---|
| nsv467634 | Chr.11:511805 - 619789 on Build GRCh38 | Loss |
 PHRF1
LOC101059906
LRRC56
MIR210HG
MIR210
RASSF7
IRF7
LMNTD2
HRAS
LOC143666
CDHR5
|
| nsv527327 | Chr.11:295343 - 620599 on Build GRCh38 | Loss |
PGGHG
IFITM5
ANO9
RNH1
B4GALNT4
IFITM3
MIR210
PKP3
CDHR5
PHRF1
SIGIRR
LOC101059906
LRRC56
MIR210HG
IFITM2
PTDSS2
RASSF7
IRF7
LMNTD2
HRAS
LOC143666
IFITM1
|
| nsv951270 | Chr.11:528401 - 628100 on Build GRCh38 | Deletion |
PHRF1
LOC101059906
LRRC56
MIR210HG
MIR210
RASSF7
IRF7
SCT
LMNTD2
HRAS
LOC143666
CDHR5
|
| nsv469923 | Chr.11:378188 - 1302334 on Build GRCh38 | Loss |
CHID1
PNPLA2
RNH1
AP2A2
MIR6744
B4GALNT4
PKP3
SIGIRR
LOC101059906
LRRC56
PANO1
CD151
IRF7
SCT
LMNTD2
TOLLIP
MUC2
CRACR2B
SNORA52
SLC25A22
ANO9
POLR2L
MUC5AC
MUC5B
TMEM80
MIR210
DEAF1
TSPAN4
MUC6
CDHR5
PHRF1
LOC101927503
LOC171391
TALDO1
EPS8L2
MIR210HG
RPLP2
PTDSS2
RASSF7
HRAS
DRD4
PDDC1
PIDD1
CEND1
LOC143666
|
| esv2759794 | Chr.11:409846 - 1336162 on Build GRCh38 | Loss |
CHID1
PNPLA2
RNH1
AP2A2
MIR6744
SIGIRR
LOC101059906
LRRC56
PANO1
CD151
IRF7
TOLLIP-AS1
SCT
LMNTD2
TOLLIP
MUC2
CRACR2B
SNORA52
SLC25A22
ANO9
POLR2L
MUC5AC
MUC5B
TMEM80
MIR210
DEAF1
TSPAN4
MUC6
CDHR5
PHRF1
LOC101927503
LOC171391
TALDO1
EPS8L2
MIR210HG
RPLP2
PTDSS2
RASSF7
HRAS
DRD4
PDDC1
PIDD1
CEND1
LOC143666
|
| nsv1053964 | Chr.11:491334 - 692433 on Build GRCh38 | Gain |
RNH1
MIR210
DEAF1
CDHR5
PHRF1
LOC101059906
LRRC56
MIR210HG
PTDSS2
RASSF7
IRF7
SCT
LMNTD2
HRAS
DRD4
LOC143666
|
| dgv182e199 | Chr.11:349830 - 943372 on Build GRCh38 | Deletion |
CHID1
PNPLA2
RNH1
AP2A2
B4GALNT4
PKP3
SIGIRR
LOC101059906
LRRC56
PANO1
CD151
IRF7
SCT
LMNTD2
CRACR2B
SNORA52
SLC25A22
ANO9
POLR2L
TMEM80
MIR210
DEAF1
TSPAN4
CDHR5
PHRF1
LOC171391
TALDO1
EPS8L2
MIR210HG
RPLP2
PTDSS2
RASSF7
HRAS
DRD4
PDDC1
PIDD1
CEND1
LOC143666
|
| nsv1159791 | Chr.11:461793 - 909492 on Build GRCh38 | Deletion |
CHID1
PNPLA2
RNH1
LOC101059906
LRRC56
PANO1
CD151
IRF7
SCT
LMNTD2
CRACR2B
SNORA52
SLC25A22
POLR2L
TMEM80
MIR210
DEAF1
TSPAN4
CDHR5
PHRF1
LOC171391
TALDO1
EPS8L2
MIR210HG
RPLP2
PTDSS2
RASSF7
HRAS
DRD4
PDDC1
PIDD1
CEND1
LOC143666
|
| nsv552855 | Chr.11:532923 - 545087 on Build GRCh38 | Loss |
LRRC56
HRAS
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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