Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.27920297C= , CM000675.2:g.27920297C= | GRCh38 |
| NC_000013.10:g.28494434C= , CM000675.1:g.28494434C= | GRCh37 |
| NC_000013.9:g.27392434C= | NCBI36 |
| NG_008183.1:g.5267C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381033.5:c.159C= (PDX1) MANE Select | ENSP00000370421.4:p.Ala53= | |
| ENST00000381033.4:c.159C= (PDX1) | ENSP00000370421.4:p.Ala53= | |
| NM_000209.3:c.159C= (PDX1) | NP_000200.1:p.Ala53= | |
| NR_047484.1:n.241+867G= (PLUT) | ||
| XR_941578.1:n.304C= (PDX1) | ||
| XR_941579.1:n.304C= (PDX1) | ||
| XR_941580.1:n.304C= (PDX1) | ||
| XR_941578.2:n.316C= (PDX1) | ||
| XR_941580.2:n.316C= (PDX1) | ||
| NM_000209.4:c.159C= (PDX1) MANE Select | NP_000200.1:p.Ala53= |