Revel Score:
ENST00000546054
0.910
ENST00000370225 (MANE Select)
0.910
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94019692T>G , CM000663.2:g.94019692T>G | GRCh38 |
| NC_000001.10:g.94485248T>G , CM000663.1:g.94485248T>G | GRCh37 |
| NC_000001.9:g.94257836T>G | NCBI36 |
| NG_009073.1:g.106458A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.5086A>C MANE Select | ENSP00000359245.3:p.Ser1696Arg | |
| ENST00000370225.3:c.5086A>C | ENSP00000359245.3:p.Ser1696Arg | |
| ENST00000460514.1:n.580A>C | ||
| ENST00000470771.1:n.196A>C | ||
| ENST00000536513.5:c.1462A>C | ENSP00000439707.2:p.Ser488Arg | |
| NM_000350.2:c.5086A>C | NP_000341.2:p.Ser1696Arg | |
| NM_000350.3:c.5086A>C MANE Select | NP_000341.2:p.Ser1696Arg |