Revel Score:
ENST00000355710 (MANE Select)
0.646
ENST00000340058
0.646
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.43126647A>C , CM000672.2:g.43126647A>C | GRCh38 |
| NC_000010.10:g.43622095A>C , CM000672.1:g.43622095A>C | GRCh37 |
| NC_000010.9:g.42942101A>C | NCBI36 |
| NG_007489.1:g.54579A>C , LRG_518:g.54579A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000615310.5:c.2716A>C | ENSP00000480088.2:p.Thr906Pro | |
| ENST00000683007.1:n.2686A>C | ||
| ENST00000340058.6:c.3112A>C | ENSP00000344798.4:p.Thr1038Pro | |
| ENST00000355710.8:c.3112A>C MANE Select | ENSP00000347942.3:p.Thr1038Pro | |
| ENST00000671844.1:c.*1706A>C | ENSP00000500541.1:n.*1706A>C | |
| ENST00000672389.1:c.*1706A>C | ENSP00000500252.1:n.*1706A>C | |
| ENST00000340058.5:c.3112A>C | ENSP00000344798.4:p.Thr1038Pro | |
| ENST00000355710.7:c.3112A>C | ENSP00000347942.3:p.Thr1038Pro | |
| ENST00000615310.4:c.*461A>C | ENSP00000480088.1:n.*461A>C | |
| NM_020630.4:c.3112A>C , LRG_518t2:c.3112A>C | NP_065681.1:p.Thr1038Pro | |
| NM_020975.4:c.3112A>C , LRG_518t1:c.3112A>C | NP_066124.1:p.Thr1038Pro | |
| XM_011540027.1:c.3112A>C | XP_011538329.1:p.Thr1038Pro | |
| NM_001355216.1:c.2350A>C | NP_001342145.1:p.Thr784Pro | |
| NM_020630.5:c.3112A>C | NP_065681.1:p.Thr1038Pro | |
| NM_020975.5:c.3112A>C | NP_066124.1:p.Thr1038Pro | |
| NM_020975.6:c.3112A>C MANE Select | NP_066124.1:p.Thr1038Pro | |
| NM_020630.6:c.3112A>C | NP_065681.1:p.Thr1038Pro |