Revel Score:
ENST00000377833 (MANE Select)
0.377
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.17019886G>C , CM000672.2:g.17019886G>C | GRCh38 |
| NC_000010.10:g.17061885G>C , CM000672.1:g.17061885G>C | GRCh37 |
| NC_000010.9:g.17101891G>C | NCBI36 |
| NG_008967.1:g.114932C>G , LRG_540:g.114932C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377833.10:c.4115C>G MANE Select | ENSP00000367064.4:p.Thr1372Arg | |
| ENST00000377833.8:c.4115C>G | ENSP00000367064.4:p.Thr1372Arg | |
| NM_001081.3:c.4115C>G , LRG_540t1:c.4115C>G | NP_001072.2:p.Thr1372Arg | |
| XM_011519708.1:c.4115C>G | XP_011518010.1:p.Thr1372Arg | |
| XM_011519709.1:c.101C>G | XP_011518011.1:p.Thr34Arg | |
| XM_011519710.1:c.77C>G | XP_011518012.1:p.Thr26Arg | |
| XM_011519708.2:c.4115C>G | XP_011518010.1:p.Thr1372Arg | |
| XM_011519709.2:c.101C>G | XP_011518011.1:p.Thr34Arg | |
| XM_011519710.2:c.77C>G | XP_011518012.1:p.Thr26Arg | |
| NM_001081.4:c.4115C>G MANE Select | NP_001072.2:p.Thr1372Arg |