Revel Score:
ENST00000360256 (MANE Select)
0.705
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154931654G>T , CM000685.2:g.154931654G>T | GRCh38 |
| NC_000023.10:g.154159929G>T , CM000685.1:g.154159929G>T | GRCh37 |
| NC_000023.9:g.153813123G>T | NCBI36 |
| NG_011403.1:g.96070C>A | |
| NG_011403.2:g.96070C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.2136C>A MANE Select | ENSP00000353393.4:p.His712Gln | |
| ENST00000647125.1:c.*1802C>A | ENSP00000496062.1:n.*1802C>A | |
| ENST00000360256.8:c.2136C>A | ENSP00000353393.4:p.His712Gln | |
| NM_000132.3:c.2136C>A | NP_000123.1:p.His712Gln | |
| XM_011531126.1:c.2031C>A | XP_011529428.1:p.His677Gln | |
| NM_000132.4:c.2136C>A MANE Select | NP_000123.1:p.His712Gln |