Revel Score:
ENST00000264381 (MANE Select)
0.688
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.165830058A>T , CM000665.2:g.165830058A>T | GRCh38 |
| NC_000003.11:g.165547846A>T , CM000665.1:g.165547846A>T | GRCh37 |
| NC_000003.10:g.167030540A>T | NCBI36 |
| NG_009031.1:g.12408T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264381.8:c.976T>A MANE Select | ENSP00000264381.3:p.Phe326Ile | |
| ENST00000264381.7:c.976T>A | ENSP00000264381.3:p.Phe326Ile | |
| ENST00000479451.5:c.107+7256T>A | ENSP00000418325.1:n.107+7256T>A | |
| ENST00000482958.1:c.976T>A | ENSP00000419804.1:p.Phe326Ile | |
| ENST00000488954.1:c.107+7256T>A | ENSP00000418504.1:n.107+7256T>A | |
| ENST00000497011.5:c.976T>A | ENSP00000419505.1:p.Phe326Ile | |
| NM_000055.2:c.976T>A | NP_000046.1:p.Phe326Ile | |
| XM_005247685.1:c.1099T>A | XP_005247742.1:p.Phe367Ile | |
| NM_000055.3:c.976T>A | NP_000046.1:p.Phe326Ile | |
| NR_137635.1:n.159+7256T>A | ||
| NR_137636.1:n.1143T>A | ||
| NM_000055.4:c.976T>A MANE Select | NP_000046.1:p.Phe326Ile | |
| NR_137635.2:n.110+7256T>A | ||
| NR_137636.2:n.1094T>A |