DNA to RNA Transcription Tool
Convert coding or template DNA into an RNA sequence with explicit strand direction.
Your result, clearly explained
Paste a sequence or load the example, then run the tool. Your sequence stays in this browser.
How to use
- Enter DNA
Paste raw DNA or a single FASTA record.
- Identify the strand
Choose coding 5′→3′, template 3′→5′, or template 5′→3′.
- Generate RNA
Read the RNA output in the 5′→3′ direction and export it.
Why ToolerWork?
Sequence calculations run inside your browser.
Strand direction, code table and approximation limits are explained.
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Why use this tool?
- Avoid confusing coding and template DNA.
- Keep strand orientation explicit in your transcription workflow.
- Preserve IUPAC ambiguity codes instead of inventing bases.
Method & assumptions
For coding DNA, T is replaced by U. A template entered 3′→5′ is complemented; a template entered 5′→3′ is reverse-complemented. The output is always RNA in the 5′→3′ direction. This is a sequence transformation, without splicing, capping or polyadenylation.
References: NCBI genetic codes
Explore all 10 biology tools →Frequently asked questions
Is DNA to RNA just replacing T with U?
That is correct for the coding strand. A template strand must also be complemented, and reversed if entered 5′→3′.
Which direction is the RNA output?
The output is always written 5′→3′. Choose the direction of your input template carefully.
Does this produce mature mRNA?
Only if your input already represents the appropriate processed coding sequence. The tool does not remove introns or add a cap or poly-A tail.
Are ambiguous DNA letters supported?
Yes. IUPAC ambiguity letters are preserved or complemented according to the selected strand mode. N remains N.
Why is U rejected in my DNA input?
DNA input uses T. Accepting U silently could hide a sequence-type mistake. Use the RNA Sequence Analyzer for existing RNA.