Revel Score:
ENST00000216271 (MANE Select)
0.652
ENST00000448072
0.652
ENST00000349505
0.652
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50249919A>C , CM000684.2:g.50249919A>C | GRCh38 |
| NC_000022.10:g.50688348A>C , CM000684.1:g.50688348A>C | GRCh37 |
| NC_000022.9:g.49030475A>C | NCBI36 |
| NG_029758.1:g.6487T>G | |
| NG_032160.1:g.53T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216271.10:c.435T>G (HDAC10) MANE Select | ENSP00000216271.5:p.Cys145Trp | |
| ENST00000216271.9:c.435T>G (HDAC10) | ENSP00000216271.5:p.Cys145Trp | |
| ENST00000349505.4:c.435T>G (HDAC10) | ENSP00000343540.4:p.Cys145Trp | |
| ENST00000415993.5:c.*47T>G (HDAC10) | ENSP00000397517.1:n.*47T>G | |
| ENST00000429374.5:c.*47T>G (HDAC10) | ENSP00000407640.1:n.*47T>G | |
| ENST00000448072.5:c.435T>G (HDAC10) | ENSP00000397542.1:p.Cys145Trp | |
| ENST00000454936.5:c.435T>G (HDAC10) | ENSP00000406150.1:p.Cys145Trp | |
| ENST00000470965.1:n.759T>G (HDAC10) | ||
| ENST00000483222.5:n.420T>G (HDAC10) | ||
| ENST00000488270.1:n.239T>G (HDAC10) | ||
| ENST00000489424.5:n.699T>G (HDAC10) | ||
| ENST00000496909.5:n.264T>G (HDAC10) | ||
| ENST00000497036.5:n.4548T>G (MAPK12) | ||
| ENST00000498366.5:n.544T>G (HDAC10) | ||
| ENST00000626012.2:c.*47T>G (HDAC10) | ENSP00000486864.1:n.*47T>G | |
| NM_001159286.1:c.435T>G (HDAC10) | NP_001152758.1:p.Cys145Trp | |
| NM_032019.5:c.435T>G (HDAC10) | NP_114408.3:p.Cys145Trp | |
| NM_032019.6:c.435T>G (HDAC10) MANE Select | NP_114408.3:p.Cys145Trp | |
| NM_001159286.2:c.435T>G (HDAC10) | NP_001152758.1:p.Cys145Trp |