Description
ARHGAP29 antisense RNA 1 [Source:HGNC Symbol;Acc:HGNC:54311]
Location
Chromosome 1: 94,247,819-94,411,036 forward strand.
GRCh38:CM000663.2
About this gene
This gene has 11 transcripts (splice variants).
Transcripts
| Transcript ID | Name | bp | Protein | Translation ID | Biotype | CCDS | RefSeq Match | Flags |
|---|---|---|---|---|---|---|---|---|
| ENST00000656153.1 | ARHGAP29-AS1-205 | 1444 | No protein | - | lncRNA | - | A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, | |
| ENST00000666276.1 | ARHGAP29-AS1-211 | 1603 | No protein | - | lncRNA | - | The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, | |
| ENST00000654057.3 | ARHGAP29-AS1-203 | 1275 | No protein | - | lncRNA | - | - | |
| ENST00000654754.1 | ARHGAP29-AS1-204 | 996 | No protein | - | lncRNA | - | - | |
| ENST00000657152.1 | ARHGAP29-AS1-206 | 952 | No protein | - | lncRNA | - | - | |
| ENST00000662164.1 | ARHGAP29-AS1-209 | 939 | No protein | - | lncRNA | - | The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, | |
| ENST00000413103.3 | ARHGAP29-AS1-201 | 887 | No protein | - | lncRNA | - | TSL 5: A transcript where no single transcript supports the model structure. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:5, | |
| ENST00000418242.3 | ARHGAP29-AS1-202 | 861 | No protein | - | lncRNA | - | TSL 5: A transcript where no single transcript supports the model structure. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:5, | |
| ENST00000665417.1 | ARHGAP29-AS1-210 | 852 | No protein | - | lncRNA | - | The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, | |
| ENST00000660527.1 | ARHGAP29-AS1-208 | 808 | No protein | - | lncRNA | - | The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, | |
| ENST00000660441.1 | ARHGAP29-AS1-207 | 767 | No protein | - | lncRNA | - | - |
