Revel Score:
ENST00000232975 (MANE Select)
0.436
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.52454008T>A , CM000665.2:g.52454008T>A | GRCh38 |
| NC_000003.11:g.52488024T>A , CM000665.1:g.52488024T>A | GRCh37 |
| NC_000003.10:g.52463064T>A | NCBI36 |
| NG_008963.1:g.5034A>T , LRG_378:g.5034A>T | |
| NG_033112.1:g.3501T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000232975.8:c.8A>T MANE Select | ENSP00000232975.3:p.Asp3Val | |
| ENST00000232975.7:c.8A>T | ENSP00000232975.3:p.Asp3Val | |
| NM_003280.2:c.8A>T , LRG_378t1:c.8A>T | NP_003271.1:p.Asp3Val | |
| NM_003280.3:c.8A>T MANE Select | NP_003271.1:p.Asp3Val |