Assay Details
Target Gene Details
| Entrez Gene ID: | 3190 | 
| Gene Name: | heterogeneous nuclear ribonucleoprotein K | 
| Gene Aliases: | AUKS, CSBP, HNRPK, TUNP | 
| Location: | Chr.9:83968083-83980782 on Build GRCh38 | 
| Assay Gene Location: | Overlaps Intron 7 - Exon 8 | 
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID | 
|---|---|---|---|---|
| HNRNPK | NM_001318186.1 | NP_001305115.1 | ||
| NM_001318187.1 | NP_001305116.1 | |||
| NM_001318188.1 | NP_001305117.1 | |||
| NM_002140.4 | NP_002131.2 | |||
| NM_031262.3 | NP_112552.1 | |||
| NM_031263.3 | NP_112553.1 | |||
| XM_005251960.2 | XP_005252017.1 | |||
| XM_005251963.3 | XP_005252020.1 | |||
| XM_005251965.2 | XP_005252022.1 | |||
| XM_011518616.1 | XP_011516918.1 | |||
| XM_017014668.1 | XP_016870157.1 | |||
| XM_017014669.1 | XP_016870158.1 | |||
| AB209562.1 | BAD92799.1 | |||
| AB451263.1 | ||||
| AB451390.1 | ||||
| AK096385.1 | ||||
| AK123117.1 | 1 | 1198 | ||
| AK291336.1 | ||||
| AK294067.1 | ||||
| AK300744.1 | ||||
| AK307962.1 | ||||
| AY911506.1 | AAW84289.1 | |||
| BC000355.2 | AAH00355.1 | |||
| BC014980.1 | AAH14980.1 | |||
| CR456771.1 | CAG33052.1 | |||
| DA394419.1 | ||||
| DC318847.1 | ||||
| DC407458.1 | ||||
| S74678.1 | AAB20770.1 | |||
| X72727.1 | CAA51267.1 | 
Target Copy Number Variation Details
| DGV Version: | Release date: 2016-05-15, GRCh GRCh38 | 
| Target Variation | Location | CNV Subtype | Genes | 
|---|---|---|---|
| nsv831644 | Chr.9:83919395 - 84089480 on Build GRCh38 | Gain |  MIR7-1  KIF27  C9orf64  LOC105376335  HNRNPK  RMI1  LOC101927575 | 
| esv2759701 | Chr.9:83799109 - 83988687 on Build GRCh38 | Gain |  MIR7-1  GKAP1  KIF27  C9orf64  LOC105376335  HNRNPK  RMI1 | 
| nsv1043703 | Chr.9:83931002 - 83988630 on Build GRCh38 | Gain |  MIR7-1  C9orf64  HNRNPK  RMI1 | 
| esv3620911 | Chr.9:83964468 - 83975773 on Build GRCh38 | Gain |  MIR7-1  HNRNPK | 
| nsv8541 | Chr.9:83854808 - 83978843 on Build GRCh38 | Gain |  MIR7-1  KIF27  C9orf64  LOC105376335  HNRNPK | 
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| Set Membership: |  Intragenic  Non-exonic  DGV Variation | 
Panther Classification:
Gene Ontology Categories:
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