Revel Score:
ENST00000264870 (MANE Select)
0.222
ENST00000441301
0.222
ENST00000414279
0.222
ENST00000431222
0.222
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.6318562C>G , CM000668.2:g.6318562C>G | GRCh38 |
| NC_000006.11:g.6318795C>G , CM000668.1:g.6318795C>G | GRCh37 |
| NC_000006.10:g.6263794C>G | NCBI36 |
| NG_008107.1:g.7130G>C , LRG_549:g.7130G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264870.8:c.103G>C MANE Select | ENSP00000264870.3:p.Val35Leu | |
| ENST00000264870.7:c.103G>C | ENSP00000264870.3:p.Val35Leu | |
| ENST00000414279.5:c.103G>C | ENSP00000413334.1:p.Val35Leu | |
| ENST00000431222.6:c.265G>C | ENSP00000416295.2:p.Val89Leu | |
| ENST00000451619.1:c.177G>C | ||
| NM_000129.3:c.103G>C , LRG_549t1:c.103G>C | NP_000120.2:p.Val35Leu | |
| XM_006715010.2:c.103G>C | XP_006715073.1:p.Val35Leu | |
| XM_011514342.1:c.265G>C | XP_011512644.1:p.Val89Leu | |
| NM_000129.4:c.103G>C MANE Select | NP_000120.2:p.Val35Leu |