Alpha-1 Antitrypsin Protein Phenotype Panel, Serum/Plasma
This blood test identifies the forms of alpha-1 antitrypsin protein in your blood and helps evaluate inherited alpha-1 antitrypsin deficiency.
["The test helps determine whether you have an inherited alpha-1 antitrypsin variant that could affect lung or liver health."]
Key facts at a glance
- LOINC
- 102082-5
- Short code
- A1AT Proteotype panel SerPl
- Synonyms
- A1AT Proteotype panel SerPl
- Category
- liver
- Sample
- serum
- Container
- Red-top tube (SST)
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Specimen volume
- 5 mL
- Stability
- Room temperature: 4h, Refrigerated: 24h, Frozen: 7d
- Hemolysis max
- 500
- Lipemia max
- 1000
- Icterus max
- 500
- TAT
- 4–24 hours
- Order
- routine
What is this test?
Alpha-1 antitrypsin is a protein that helps protect the lungs from inflammation. This test identifies the different forms, or phenotypes, of the protein present in your blood.
Why might I need this test?
This test may be ordered if you have low alpha-1 antitrypsin levels, unexplained chronic lung disease, unexplained liver disease, or a family history of alpha-1 antitrypsin deficiency. It can also help assess the risk to relatives.
How is the test performed?
A blood sample is collected, and the laboratory analyzes the alpha-1 antitrypsin protein pattern to determine your phenotype. If the result is unclear or suggests a rare variant, the laboratory may recommend additional testing.
How do I prepare for the test?
No special preparation is usually needed. Tell your healthcare professional if you have a bleeding disorder or are taking medicines that increase bleeding risk, and follow any instructions provided by the laboratory.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
An abnormal phenotype may indicate an inherited alpha-1 antitrypsin variant associated with reduced protective protein levels. Such variants can increase the risk of emphysema and certain liver conditions, particularly when a person also has environmental liver injury. A phenotype result should be interpreted with alpha-1 antitrypsin level measurements, other laboratory results, and your medical history.
Short name
Alpha-1 Antitrypsin Phenotype Panel
Frequently asked questions
Does this test measure how much alpha-1 antitrypsin is present?
Is alpha-1 antitrypsin deficiency inherited?
Do I need genetic testing to confirm the result?
Sources
- 1
- 2Lab Tests OnlineSource
- 3
Click any link to access the full source. PubMed Central (PMC) links provide free full-text access.
This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy