Revel Score:
ENST00000256958 (MANE Select)
0.447
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21176783T>A , CM000674.2:g.21176783T>A | GRCh38 |
| NC_000012.11:g.21329717T>A , CM000674.1:g.21329717T>A | GRCh37 |
| NC_000012.10:g.21220984T>A | NCBI36 |
| NG_011745.1:g.50590T>A , LRG_1022:g.50590T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256958.3:c.367T>A MANE Select | ENSP00000256958.2:p.Tyr123Asn | |
| ENST00000256958.2:c.367T>A | ENSP00000256958.2:p.Tyr123Asn | |
| ENST00000543498.5:c.433T>A | ||
| NM_006446.4:c.367T>A , LRG_1022t1:c.367T>A | NP_006437.3:p.Tyr123Asn | |
| NM_006446.5:c.367T>A MANE Select | NP_006437.3:p.Tyr123Asn |