Revel Score:
ENST00000378802 (MANE Select)
0.615
ENST00000274118
0.615
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186208954T>A , CM000666.2:g.186208954T>A | GRCh38 |
| NC_000004.11:g.187130108T>A , CM000666.1:g.187130108T>A | GRCh37 |
| NC_000004.10:g.187367102T>A | NCBI36 |
| NG_007965.1:g.22435T>A | |
| NG_012095.2:g.4976T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378802.5:c.1180T>A MANE Select | ENSP00000368079.4:p.Ser394Thr | |
| ENST00000378802.4:c.1180T>A | ENSP00000368079.4:p.Ser394Thr | |
| ENST00000502665.1:n.415T>A | ||
| ENST00000507209.5:n.5878T>A | ||
| ENST00000513354.5:n.270T>A | ||
| NM_207352.3:c.1180T>A | NP_997235.3:p.Ser394Thr | |
| XM_005262935.2:c.1180T>A | XP_005262992.1:p.Ser394Thr | |
| XM_006714184.2:c.784T>A | XP_006714247.1:p.Ser262Thr | |
| XM_005262935.4:c.1180T>A | XP_005262992.1:p.Ser394Thr | |
| XM_017008037.1:c.784T>A | XP_016863526.1:p.Ser262Thr | |
| NM_207352.4:c.1180T>A MANE Select | NP_997235.3:p.Ser394Thr |