Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.68653304T>C , CM000664.2:g.68653304T>C | GRCh38 |
| NC_000002.11:g.68880436T>C , CM000664.1:g.68880436T>C | GRCh37 |
| NC_000002.10:g.68733940T>C | NCBI36 |
| NG_051312.1:g.14717T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_138964.4:c.486-1576T>C (PROKR1) MANE Select | NP_620414.1:n.486-1576T>C |
| ENST00000303786.5:c.486-1576T>C (PROKR1) MANE Select | ENSP00000303775.4:n.486-1576T>C |
| NM_138964.2:c.486-1576T>C (PROKR1) | NP_620414.1:n.486-1576T>C |
| NM_138964.3:c.486-1576T>C (PROKR1) | NP_620414.1:n.486-1576T>C |
| ENST00000303786.4:c.486-1576T>C (PROKR1) | ENSP00000303775.3:n.486-1576T>C |
| ENST00000394342.2:c.486-1576T>C (APLF) | ENSP00000377874.2:n.486-1576T>C |
| ENST00000627740.1:n.1198-1576T>C (APLF) |