Revel Score:
ENST00000345060 (MANE Select)
0.264
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37965578T>C , CM000670.2:g.37965578T>C | GRCh38 |
| NC_000008.10:g.37823096T>C , CM000670.1:g.37823096T>C | GRCh37 |
| NC_000008.9:g.37942253T>C | NCBI36 |
| NG_011936.1:g.6089A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000345060.5:c.892A>G MANE Select | ENSP00000343782.3:p.Met298Val | |
| ENST00000520341.2:n.1020A>G | ||
| ENST00000647937.1:c.376A>G | ENSP00000497740.1:p.Met126Val | |
| ENST00000345060.4:c.892A>G | ENSP00000343782.3:p.Met298Val | |
| ENST00000520341.1:n.167A>G | ||
| ENST00000614635.1:c.892A>G | ENSP00000480325.1:p.Met298Val | |
| NM_000025.2:c.892A>G | NP_000016.1:p.Met298Val | |
| NM_000025.3:c.892A>G MANE Select | NP_000016.1:p.Met298Val |