Revel Score:
ENST00000369295 (MANE Select)
0.025
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.114044286C>T , CM000672.2:g.114044286C>T | GRCh38 |
| NC_000010.10:g.115804045C>T , CM000672.1:g.115804045C>T | GRCh37 |
| NC_000010.9:g.115794035C>T | NCBI36 |
| NG_012187.1:g.5240C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369295.4:c.154C>T MANE Select | ENSP00000358301.2:p.Pro52Ser | |
| ENST00000369295.3:c.154C>T | ENSP00000358301.2:p.Pro52Ser | |
| NM_000684.2:c.154C>T | NP_000675.1:p.Pro52Ser | |
| NM_000684.3:c.154C>T MANE Select | NP_000675.1:p.Pro52Ser |