Revel Score:
ENST00000270142 (MANE Select)
0.893
ENST00000389995
0.893
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.31667337C>T , CM000683.2:g.31667337C>T | GRCh38 |
| NC_000021.8:g.33039650C>T , CM000683.1:g.33039650C>T | GRCh37 |
| NC_000021.7:g.31961521C>T | NCBI36 |
| NG_008689.1:g.12716C>T , LRG_652:g.12716C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270142.11:c.319C>T MANE Select | ENSP00000270142.7:p.Leu107Phe | |
| ENST00000270142.10:c.319C>T | ENSP00000270142.6:p.Leu107Phe | |
| ENST00000389995.4:c.262C>T | ENSP00000374645.4:p.Leu88Phe | |
| ENST00000470944.1:n.1247C>T | ||
| ENST00000476106.5:n.582C>T | ||
| NM_000454.4:c.319C>T , LRG_652t1:c.319C>T | NP_000445.1:p.Leu107Phe | |
| NM_000454.5:c.319C>T MANE Select | NP_000445.1:p.Leu107Phe |