CPA2
carboxypeptidase A2
Summary
Three different forms of human pancreatic procarboxypeptidase A have been isolated. The encoded protein represents the A2 form, which is a monomeric protein with different biochemical properties from the A1 and A3 forms. The A2 form of pancreatic procarboxypeptidase acts on aromatic C-terminal residues and is a secreted protein. [provided by RefSeq, Dec 2008]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs200908002 | 7:129,906,765 | A/G | — | uncertain significance |
| rs199695765 | 7:129,908,848 | C/T | stop gained | — |
| rs149013286 | 7:129,909,553 | C/T | — | benign |
| rs61997065 | 7:129,909,554 | G/A | — | benign |
| rs749226338 | 7:129,909,569 | G/A | — | uncertain significance |
| rs1239669548 | 7:129,909,606 | A/G | — | uncertain significance |
| rs751540588 | 7:129,909,638 | G/A | — | uncertain significance |
| rs377750328 | 7:129,910,549 | A/T | — | uncertain significance |
| rs756399806 | 7:129,912,936 | C/G | — | uncertain significance |
| rs748413926 | 7:129,912,940 | G/A | — | uncertain significance |
| rs374786646 | 7:129,912,955 | G/T | — | uncertain significance |
| rs139150196 | 7:129,912,965 | G/A | — | uncertain significance |
| rs762396446 | 7:129,912,974 | A/T | — | uncertain significance |
| rs10257530 | 7:129,913,520 | T/C | regulatory region variant | — |
| rs61731658 | 7:129,915,016 | A/G | — | benign |
| rs1584734619 | 7:129,915,017 | T/C | — | uncertain significance |
| rs2535682817 | 7:129,915,035 | T/C | — | uncertain significance |
| rs754626497 | 7:129,915,044 | G/A | — | uncertain significance |
| rs1264021831 | 7:129,916,480 | T/C | — | uncertain significance |
| rs79082583 | 7:129,916,501 | A/G | — | uncertain significance |
| rs201088138 | 7:129,916,538 | C/T | — | uncertain significance |
| rs201623522 | 7:129,917,670 | G/A | — | uncertain significance |
| rs767056608 | 7:129,917,688 | G/C | — | uncertain significance |
| rs765808838 | 7:129,917,695 | G/T | — | uncertain significance |
| rs754895713 | 7:129,917,717 | G/A | — | uncertain significance |
| rs369196272 | 7:129,919,380 | A/G | — | uncertain significance |
| rs1264209202 | 7:129,919,392 | A/G | — | uncertain significance |
| rs774916145 | 7:129,921,962 | G/C | — | uncertain significance |
| rs557844120 | 7:129,921,987 | A/C | — | uncertain significance |
| rs767478523 | 7:129,921,989 | G/A | — | uncertain significance |
| rs199962603 | 7:129,929,541 | T/C | — | uncertain significance |
| rs562556003 | 7:129,929,555 | A/G | — | uncertain significance |
| rs1353276991 | 7:129,929,560 | G/A | — | uncertain significance |
| rs377236326 | 7:129,929,571 | G/A | — | uncertain significance |
| rs370431439 | 7:129,929,583 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.