Revel Score:
ENST00000260682 (MANE Select)
0.731
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94988922T>C , CM000672.2:g.94988922T>C | GRCh38 |
| NC_000010.10:g.96748679T>C , CM000672.1:g.96748679T>C | GRCh37 |
| NC_000010.9:g.96738669T>C | NCBI36 |
| NG_008385.1:g.55265T>C | |
| NG_008385.2:g.55765T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.1367T>C MANE Select | ENSP00000260682.6:p.Phe456Ser | |
| ENST00000643112.1:c.*376T>C | ENSP00000496202.1:n.*376T>C | |
| ENST00000260682.6:c.1367T>C | ENSP00000260682.6:p.Phe456Ser | |
| NM_000771.3:c.1367T>C | NP_000762.2:p.Phe456Ser | |
| NM_000771.4:c.1367T>C MANE Select | NP_000762.2:p.Phe456Ser |