Revel Score:
ENST00000377833 (MANE Select)
0.699
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.17045102A>C , CM000672.2:g.17045102A>C | GRCh38 |
| NC_000010.10:g.17087101A>C , CM000672.1:g.17087101A>C | GRCh37 |
| NC_000010.9:g.17127107A>C | NCBI36 |
| NG_008967.1:g.89716T>G , LRG_540:g.89716T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377833.10:c.3577T>G MANE Select | ENSP00000367064.4:p.Trp1193Gly | |
| ENST00000377833.8:c.3577T>G | ENSP00000367064.4:p.Trp1193Gly | |
| NM_001081.3:c.3577T>G , LRG_540t1:c.3577T>G | NP_001072.2:p.Trp1193Gly | |
| XM_011519708.1:c.3577T>G | XP_011518010.1:p.Trp1193Gly | |
| XM_011519708.2:c.3577T>G | XP_011518010.1:p.Trp1193Gly | |
| NM_001081.4:c.3577T>G MANE Select | NP_001072.2:p.Trp1193Gly |