Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.43567281C= , CM000668.2:g.43567281C= | GRCh38 |
| NC_000006.11:g.43535018C= , CM000668.1:g.43535018C= | GRCh37 |
| NC_000006.10:g.43642996C= | NCBI36 |
| NG_051658.1:g.13795G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_020750.3:c.722G= (XPO5) MANE Select | NP_065801.1:p.Ser241= |
| ENST00000265351.12:c.722G= (XPO5) MANE Select | ENSP00000265351.7:p.Ser241= |
| NM_001318876.2:c.945+38010C= (POLR1C) | NP_001305805.1:n.945+38010C= |
| NM_020750.2:c.722G= (XPO5) | NP_065801.1:p.Ser241= |
| NR_144392.1:n.933G= (XPO5) | |
| NR_144392.2:n.896G= (XPO5) | |
| ENST00000265351.11:c.722G= (XPO5) | ENSP00000265351.7:p.Ser241= |