Revel Score:
ENST00000335508 (MANE Select)
0.269
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.197400720T>G , CM000664.2:g.197400720T>G | GRCh38 |
| NC_000002.11:g.198265444T>G , CM000664.1:g.198265444T>G | GRCh37 |
| NC_000002.10:g.197973689T>G | NCBI36 |
| NG_032903.2:g.39328A>C , LRG_624:g.39328A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000335508.11:c.2713A>C MANE Select | ENSP00000335321.6:p.Thr905Pro | |
| ENST00000470268.2:n.4597A>C | ||
| ENST00000652026.1:c.*3780A>C | ENSP00000498652.1:n.*3780A>C | |
| ENST00000652738.1:c.*2972A>C | ENSP00000499119.1:n.*2972A>C | |
| ENST00000335508.10:c.2713A>C | ENSP00000335321.5:p.Thr905Pro | |
| NM_012433.2:c.2713A>C | NP_036565.2:p.Thr905Pro | |
| NM_012433.3:c.2713A>C , LRG_624t2:c.2713A>C | NP_036565.2:p.Thr905Pro | |
| XM_011510867.1:c.2275A>C | XP_011509169.1:p.Thr759Pro | |
| XM_011510868.1:c.2275A>C | XP_011509170.1:p.Thr759Pro | |
| XR_241300.2:n.2805A>C | ||
| XR_001738680.2:n.2758A>C | ||
| NM_012433.4:c.2713A>C MANE Select | NP_036565.2:p.Thr905Pro |