Genomic Map
Back To TopAssay Details
Target Gene Details
Entrez Gene ID: | 3184 |
Gene Name: | heterogeneous nuclear ribonucleoprotein D |
Gene Aliases: |
AUF1, AUF1A, HNRPD, P37, hnRNPD0 |
Location: |
Chr.4:82353314-82373996 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 2 - Exon 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| HNRNPD | NM_001003810.1 | NP_001003810.1 | ||
| NM_002138.3 | NP_002129.2 | |||
| NM_031369.2 | NP_112737.1 | |||
| NM_031370.2 | NP_112738.1 | |||
| AF039575.1 | AAB96683.1 | |||
| AK057836.1 | ||||
| AK292707.1 | ||||
| AK300149.1 | ||||
| AK303552.1 | ||||
| BC002401.1 | AAH02401.1 | |||
| BC023977.2 | AAH23977.1 | |||
| BC026015.2 | AAH26015.1 | |||
| D55671.1 | BAA09522.1 | |||
| D55672.1 | BAA09523.1 | |||
| D55673.1 | BAA09524.1 | |||
| D55674.1 | BAA09525.1 | |||
| M94630.1 | AAA35781.1 | |||
| X03910.1 | CAA27544.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv950348 | Chr.4:82359048 - 82372747 on Build GRCh38 | Duplication |
 HNRNPD
|
| nsv594743 | Chr.4:82353481 - 82404421 on Build GRCh38 | Loss |
HNRNPD
|
| nsv829988 | Chr.4:82316984 - 82489338 on Build GRCh38 | Loss |
HNRNPDL
HNRNPD
TMEM150C
LOC105377310
ENOPH1
|
Back To TopMore Information
Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
Back To Top