Revel Score:
ENST00000261405 (MANE Select)
0.626
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5981989A>T , CM000674.2:g.5981989A>T | GRCh38 |
| NC_000012.11:g.6091155A>T , CM000674.1:g.6091155A>T | GRCh37 |
| NC_000012.10:g.5961416A>T | NCBI36 |
| NG_009072.1:g.147682T>A | |
| NG_009072.2:g.147682T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261405.10:c.7084T>A MANE Select | ENSP00000261405.5:p.Cys2362Ser | |
| ENST00000261405.9:c.7084T>A | ENSP00000261405.5:p.Cys2362Ser | |
| NM_000552.3:c.7084T>A | NP_000543.2:p.Cys2362Ser | |
| NM_000552.4:c.7084T>A | NP_000543.2:p.Cys2362Ser | |
| NM_000552.5:c.7084T>A MANE Select | NP_000543.3:p.Cys2362Ser |