Revel Score:
ENST00000264381 (MANE Select)
0.211
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.165830088C>T , CM000665.2:g.165830088C>T | GRCh38 |
| NC_000003.11:g.165547876C>T , CM000665.1:g.165547876C>T | GRCh37 |
| NC_000003.10:g.167030570C>T | NCBI36 |
| NG_009031.1:g.12378G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264381.8:c.946G>A MANE Select | ENSP00000264381.3:p.Val316Ile | |
| ENST00000264381.7:c.946G>A | ENSP00000264381.3:p.Val316Ile | |
| ENST00000479451.5:c.107+7226G>A | ENSP00000418325.1:n.107+7226G>A | |
| ENST00000482958.1:c.946G>A | ENSP00000419804.1:p.Val316Ile | |
| ENST00000488954.1:c.107+7226G>A | ENSP00000418504.1:n.107+7226G>A | |
| ENST00000497011.5:c.946G>A | ENSP00000419505.1:p.Val316Ile | |
| NM_000055.2:c.946G>A | NP_000046.1:p.Val316Ile | |
| XM_005247685.1:c.1069G>A | XP_005247742.1:p.Val357Ile | |
| NM_000055.3:c.946G>A | NP_000046.1:p.Val316Ile | |
| NR_137635.1:n.159+7226G>A | ||
| NR_137636.1:n.1113G>A | ||
| NM_000055.4:c.946G>A MANE Select | NP_000046.1:p.Val316Ile | |
| NR_137635.2:n.110+7226G>A | ||
| NR_137636.2:n.1064G>A |