Revel Score:
ENST00000343257 (MANE Select)
0.982
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.143339289C>A , CM000669.2:g.143339289C>A | GRCh38 |
| NC_000007.13:g.143036382C>A , CM000669.1:g.143036382C>A | GRCh37 |
| NC_000007.12:g.142746504C>A | NCBI36 |
| NG_009815.1:g.28164C>A | |
| NG_009815.2:g.28164C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650516.2:c.1438C>A | ENSP00000498052.2:p.Pro480Thr | |
| ENST00000343257.7:c.1438C>A MANE Select | ENSP00000339867.2:p.Pro480Thr | |
| ENST00000432192.6:c.1262C>A | ||
| ENST00000343257.6:c.1438C>A | ENSP00000339867.2:p.Pro480Thr | |
| NM_000083.2:c.1438C>A | NP_000074.2:p.Pro480Thr | |
| NR_046453.1:n.1378C>A | ||
| XM_011515781.1:c.1462C>A | XP_011514083.1:p.Pro488Thr | |
| XM_011515782.1:c.184C>A | XP_011514084.1:p.Pro62Thr | |
| XM_011515782.2:c.184C>A | XP_011514084.1:p.Pro62Thr | |
| XM_017011739.1:c.1012C>A | XP_016867228.1:p.Pro338Thr | |
| XM_017011740.1:c.988C>A | XP_016867229.1:p.Pro330Thr | |
| NM_000083.3:c.1438C>A MANE Select | NP_000074.3:p.Pro480Thr | |
| NR_046453.2:n.1393C>A |