Revel Score:
ENST00000359596 (MANE Select)
0.929
ENST00000355481
0.929
ENST00000360985
0.929
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38505837A>T , CM000681.2:g.38505837A>T | GRCh38 |
| NC_000019.9:g.38996477A>T , CM000681.1:g.38996477A>T | GRCh37 |
| NC_000019.8:g.43688317A>T | NCBI36 |
| NG_008866.1:g.77138A>T , LRG_766:g.77138A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000599547.6:c.8432A>T | ENSP00000471601.2:p.Glu2811Val | |
| ENST00000359596.8:c.8432A>T MANE Select | ENSP00000352608.2:p.Glu2811Val | |
| ENST00000355481.8:c.8432A>T | ENSP00000347667.3:p.Glu2811Val | |
| ENST00000359596.7:c.8432A>T | ENSP00000352608.2:p.Glu2811Val | |
| ENST00000360985.7:c.8429A>T | ENSP00000354254.4:p.Glu2810Val | |
| ENST00000594335.5:c.1884A>T | ||
| NM_000540.2:c.8432A>T , LRG_766t1:c.8432A>T | NP_000531.2:p.Glu2811Val | |
| NM_001042723.1:c.8432A>T | NP_001036188.1:p.Glu2811Val | |
| XM_006723317.1:c.8432A>T | XP_006723380.1:p.Glu2811Val | |
| XM_006723319.1:c.8432A>T | XP_006723382.1:p.Glu2811Val | |
| XM_011527204.1:c.8429A>T | XP_011525506.1:p.Glu2810Val | |
| XM_011527205.1:c.8432A>T | XP_011525507.1:p.Glu2811Val | |
| XM_006723317.2:c.8432A>T | XP_006723380.1:p.Glu2811Val | |
| XM_006723319.2:c.8432A>T | XP_006723382.1:p.Glu2811Val | |
| XM_011527205.2:c.8432A>T | XP_011525507.1:p.Glu2811Val | |
| XR_001753735.1:n.8515A>T | ||
| NM_000540.3:c.8432A>T MANE Select | NP_000531.2:p.Glu2811Val | |
| NM_001042723.2:c.8432A>T | NP_001036188.1:p.Glu2811Val |