Revel Score:
ENST00000331134 (MANE Select)
0.418
ENST00000374747
0.418
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.81629795A>T , CM000679.2:g.81629795A>T | GRCh38 |
| NC_000017.10:g.79596821A>T , CM000679.1:g.79596821A>T | GRCh37 |
| NC_000017.9:g.77207226A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000705719.1:c.155T>A | ENSP00000516165.1:p.Val52Asp | |
| ENST00000331134.11:c.26T>A MANE Select | ENSP00000331487.5:p.Val9Asp | |
| ENST00000331134.10:c.26T>A | ENSP00000331487.5:p.Val9Asp | |
| ENST00000374747.9:c.26T>A | ENSP00000363879.5:p.Val9Asp | |
| ENST00000570300.1:n.47T>A | ||
| ENST00000574897.5:c.26T>A | ENSP00000461543.1:p.Val9Asp | |
| ENST00000625705.1:c.23T>A | ENSP00000486640.1:p.Val8Asp | |
| NM_017921.3:c.26T>A | NP_060391.2:p.Val9Asp | |
| XM_011524979.1:c.26T>A | XP_011523281.1:p.Val9Asp | |
| XM_011524980.1:c.26T>A | XP_011523282.1:p.Val9Asp | |
| XM_011524981.1:c.26T>A | XP_011523283.1:p.Val9Asp | |
| XM_011524982.1:c.26T>A | XP_011523284.1:p.Val9Asp | |
| XR_934501.1:n.244T>A | ||
| XR_934502.1:n.244T>A | ||
| XM_011524982.2:c.26T>A | XP_011523284.1:p.Val9Asp | |
| XR_001752557.1:n.244T>A | ||
| NM_017921.4:c.26T>A MANE Select | NP_060391.2:p.Val9Asp | |
| NM_001369698.1:c.26T>A | NP_001356627.1:p.Val9Asp |