Genomic Map
Back To TopAssay 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: | 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 |
|---|---|---|---|
| nsv552854 | Chr.11:511805 - 619789 on Build GRCh38 | Loss |
 CDHR5
LOC101059906
MIR210HG
LMNTD2
PHRF1
MIR210
HRAS
LOC143666
RASSF7
IRF7
LRRC56
|
| nsv527327 | Chr.11:295343 - 620599 on Build GRCh38 | Loss |
LMNTD2
SIGIRR
RNH1
IFITM1
LOC143666
RASSF7
CDHR5
LOC101059906
IFITM3
IFITM5
MIR210HG
PHRF1
PKP3
ANO9
PGGHG
MIR210
HRAS
IFITM2
B4GALNT4
IRF7
LRRC56
PTDSS2
|
| nsv951270 | Chr.11:528401 - 628100 on Build GRCh38 | Deletion |
CDHR5
LOC101059906
MIR210HG
LMNTD2
PHRF1
MIR210
HRAS
LOC143666
SCT
RASSF7
IRF7
LRRC56
|
| nsv469923 | Chr.11:378188 - 1302334 on Build GRCh38 | Loss |
LMNTD2
SIGIRR
MUC2
TSPAN4
PNPLA2
CHID1
TALDO1
CEND1
ANO9
SNORA52
RPLP2
HRAS
MUC5B
PANO1
LOC101927503
B4GALNT4
IRF7
MIR6744
PTDSS2
DRD4
MUC5AC
POLR2L
AP2A2
RNH1
LOC143666
SCT
RASSF7
PDDC1
MUC6
EPS8L2
CD151
CDHR5
CRACR2B
LOC101059906
SLC25A22
MIR210HG
PHRF1
TMEM80
PKP3
LOC171391
MIR210
PIDD1
DEAF1
LRRC56
TOLLIP
|
| esv2759794 | Chr.11:409846 - 1336162 on Build GRCh38 | Loss |
LMNTD2
SIGIRR
MUC2
TSPAN4
PNPLA2
CHID1
TALDO1
CEND1
ANO9
SNORA52
RPLP2
HRAS
MUC5B
PANO1
LOC101927503
IRF7
MIR6744
PTDSS2
DRD4
MUC5AC
TOLLIP-AS1
POLR2L
AP2A2
RNH1
LOC143666
SCT
RASSF7
PDDC1
MUC6
EPS8L2
CD151
CDHR5
CRACR2B
LOC101059906
SLC25A22
MIR210HG
PHRF1
TMEM80
LOC171391
MIR210
PIDD1
DEAF1
LRRC56
TOLLIP
|
| dgv182e199 | Chr.11:349830 - 943372 on Build GRCh38 | Deletion |
LMNTD2
SIGIRR
TSPAN4
PNPLA2
CHID1
TALDO1
CEND1
ANO9
SNORA52
RPLP2
HRAS
PANO1
B4GALNT4
IRF7
PTDSS2
DRD4
POLR2L
AP2A2
RNH1
LOC143666
SCT
RASSF7
PDDC1
EPS8L2
CD151
CDHR5
CRACR2B
LOC101059906
SLC25A22
MIR210HG
PHRF1
TMEM80
PKP3
LOC171391
MIR210
PIDD1
DEAF1
LRRC56
|
| nsv1053964 | Chr.11:491334 - 692433 on Build GRCh38 | Gain |
DRD4
LMNTD2
RNH1
LOC143666
SCT
RASSF7
CDHR5
LOC101059906
MIR210HG
PHRF1
MIR210
HRAS
IRF7
DEAF1
LRRC56
PTDSS2
|
| nsv1159791 | Chr.11:461793 - 909492 on Build GRCh38 | Deletion |
LMNTD2
TSPAN4
PNPLA2
CHID1
TALDO1
CEND1
SNORA52
RPLP2
HRAS
PANO1
IRF7
PTDSS2
DRD4
POLR2L
RNH1
LOC143666
SCT
RASSF7
PDDC1
EPS8L2
CD151
CDHR5
CRACR2B
LOC101059906
SLC25A22
MIR210HG
PHRF1
TMEM80
LOC171391
MIR210
PIDD1
DEAF1
LRRC56
|
| nsv552855 | Chr.11:532923 - 545087 on Build GRCh38 | Loss |
HRAS
LRRC56
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
Back To Top