Revel Score:
ENST00000376734 (MANE Select)
0.106
ENST00000376728
0.106
ENST00000540829
0.106
gnomAD v3:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.30108087A>T , CM000668.2:g.30108087A>T | GRCh38 |
| NC_000006.11:g.30075864A>T , CM000668.1:g.30075864A>T | GRCh37 |
| NC_000006.10:g.30183843A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376734.4:c.849T>A (TRIM31) MANE Select | ENSP00000365924.3:p.His283Gln | |
| ENST00000376734.3:c.849T>A (TRIM31) | ENSP00000365924.3:p.His283Gln | |
| ENST00000468264.1:n.113T>A (TRIM31) | ||
| ENST00000485864.5:n.539T>A (TRIM31) | ||
| NM_007028.3:c.849T>A (TRIM31) | NP_008959.3:p.His283Gln | |
| NR_126470.1:n.273+300A>T (TRIM31-AS1) | ||
| XM_011514264.1:c.846T>A (TRIM31) | XP_011512566.1:p.His282Gln | |
| XM_011514265.1:c.849T>A (TRIM31) | XP_011512567.1:p.His283Gln | |
| XM_011514266.1:c.*82T>A (TRIM31) | XP_011512568.1:n.*82T>A | |
| XR_926036.1:n.959T>A (TRIM31) | ||
| XR_926037.1:n.915T>A (TRIM31) | ||
| NM_007028.4:c.849T>A (TRIM31) | NP_008959.3:p.His283Gln | |
| NR_134870.1:n.975T>A (TRIM31) | ||
| NR_134871.1:n.908T>A (TRIM31) | ||
| NM_007028.5:c.849T>A (TRIM31) MANE Select | NP_008959.3:p.His283Gln | |
| NR_134870.2:n.959T>A (TRIM31) | ||
| NR_134871.2:n.892T>A (TRIM31) |