Revel Score:
ENST00000297350 (MANE Select)
0.449
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.118932980G>T , CM000670.2:g.118932980G>T | GRCh38 |
| NC_000008.10:g.119945219G>T , CM000670.1:g.119945219G>T | GRCh37 |
| NC_000008.9:g.120014400G>T | NCBI36 |
| NG_012202.1:g.24165C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297350.9:c.351C>A MANE Select | ENSP00000297350.4:p.Phe117Leu | |
| ENST00000297350.8:c.351C>A | ENSP00000297350.4:p.Phe117Leu | |
| ENST00000517352.1:c.351C>A | ENSP00000427924.1:p.Phe117Leu | |
| NM_002546.3:c.351C>A | NP_002537.3:p.Phe117Leu | |
| NM_002546.4:c.351C>A MANE Select | NP_002537.3:p.Phe117Leu |