Revel Score:
ENST00000438045
0.498
ENST00000248633 (MANE Select)
0.498
ENST00000428214
0.498
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.92501979G>C , CM000669.2:g.92501979G>C | GRCh38 |
| NC_000007.13:g.92131293G>C , CM000669.1:g.92131293G>C | GRCh37 |
| NC_000007.12:g.91969229G>C | NCBI36 |
| NG_008341.1:g.31553C>G | |
| NG_008341.2:g.31553C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248633.9:c.2327C>G MANE Select | ENSP00000248633.4:p.Thr776Ser | |
| ENST00000248633.8:c.2327C>G | ENSP00000248633.4:p.Thr776Ser | |
| ENST00000428214.5:c.2156C>G | ENSP00000394413.1:p.Thr719Ser | |
| ENST00000438045.5:c.1361C>G | ENSP00000410438.1:p.Thr454Ser | |
| ENST00000484913.5:n.2366C>G | ||
| ENST00000496092.1:n.125C>G | ||
| ENST00000496420.5:n.2003C>G | ||
| NM_000466.2:c.2327C>G | NP_000457.1:p.Thr776Ser | |
| NM_001282677.1:c.2156C>G | NP_001269606.1:p.Thr719Ser | |
| NM_001282678.1:c.1703C>G | NP_001269607.1:p.Thr568Ser | |
| XM_005250433.3:c.578C>G | XP_005250490.1:p.Thr193Ser | |
| XR_242246.3:n.2423C>G | ||
| XM_017012319.2:c.578C>G | XP_016867808.1:p.Thr193Ser | |
| XR_001744808.2:n.1354C>G | ||
| XR_242246.5:n.2374C>G | ||
| NM_000466.3:c.2327C>G MANE Select | NP_000457.1:p.Thr776Ser | |
| NM_001282677.2:c.2156C>G | NP_001269606.1:p.Thr719Ser | |
| NM_001282678.2:c.1703C>G | NP_001269607.1:p.Thr568Ser |