Revel Score:
ENST00000520113 (MANE Select)
0.955
ENST00000369538
0.955
ENST00000353928
0.955
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114677926A>G , CM000663.2:g.114677926A>G | GRCh38 |
| NC_000001.10:g.115220547A>G , CM000663.1:g.115220547A>G | GRCh37 |
| NC_000001.9:g.115022070A>G | NCBI36 |
| NG_008012.1:g.22630T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369538.4:c.1196T>C | ENSP00000358551.4:p.Phe399Ser | |
| ENST00000520113.7:c.1208T>C MANE Select | ENSP00000430075.3:p.Phe403Ser | |
| ENST00000637080.1:c.991T>C | ENSP00000489753.1:n.991T>C | |
| ENST00000639077.1:n.873T>C | ||
| ENST00000369538.3:c.1295T>C | ENSP00000358551.3:p.Phe432Ser | |
| ENST00000520113.6:c.1307T>C | ENSP00000430075.2:p.Phe436Ser | |
| NM_000036.2:c.1307T>C | NP_000027.2:p.Phe436Ser | |
| NM_001172626.1:c.1295T>C | NP_001166097.1:p.Phe432Ser | |
| NM_000036.3:c.1208T>C MANE Select | NP_000027.3:p.Phe403Ser | |
| NM_001172626.2:c.1196T>C | NP_001166097.2:p.Phe399Ser |