Revel Score:
ENST00000264381 (MANE Select)
0.207
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.165830038G>C , CM000665.2:g.165830038G>C | GRCh38 |
| NC_000003.11:g.165547826G>C , CM000665.1:g.165547826G>C | GRCh37 |
| NC_000003.10:g.167030520G>C | NCBI36 |
| NG_009031.1:g.12428C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264381.8:c.996C>G MANE Select | ENSP00000264381.3:p.Asp332Glu | |
| ENST00000264381.7:c.996C>G | ENSP00000264381.3:p.Asp332Glu | |
| ENST00000479451.5:c.107+7276C>G | ENSP00000418325.1:n.107+7276C>G | |
| ENST00000482958.1:c.996C>G | ENSP00000419804.1:p.Asp332Glu | |
| ENST00000488954.1:c.107+7276C>G | ENSP00000418504.1:n.107+7276C>G | |
| ENST00000497011.5:c.996C>G | ENSP00000419505.1:p.Asp332Glu | |
| NM_000055.2:c.996C>G | NP_000046.1:p.Asp332Glu | |
| XM_005247685.1:c.1119C>G | XP_005247742.1:p.Asp373Glu | |
| NM_000055.3:c.996C>G | NP_000046.1:p.Asp332Glu | |
| NR_137635.1:n.159+7276C>G | ||
| NR_137636.1:n.1163C>G | ||
| NM_000055.4:c.996C>G MANE Select | NP_000046.1:p.Asp332Glu | |
| NR_137635.2:n.110+7276C>G | ||
| NR_137636.2:n.1114C>G |