Revel Score:
ENST00000370862 (MANE Select)
0.192
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.55277539A>C , CM000668.2:g.55277539A>C | GRCh38 |
| NC_000006.11:g.55142337A>C , CM000668.1:g.55142337A>C | GRCh37 |
| NC_000006.10:g.55250296A>C | NCBI36 |
| NG_012447.1:g.108267A>C | |
| NG_012447.2:g.176080A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370862.4:c.922A>C MANE Select | ENSP00000359899.3:p.Ile308Leu | |
| ENST00000370862.3:c.922A>C | ENSP00000359899.3:p.Ile308Leu | |
| ENST00000615358.4:c.922A>C | ENSP00000477548.1:p.Ile308Leu | |
| NM_001526.3:c.922A>C | NP_001517.2:p.Ile308Leu | |
| XM_011514542.1:c.727A>C | XP_011512844.1:p.Ile243Leu | |
| NM_001526.4:c.922A>C | NP_001517.2:p.Ile308Leu | |
| XM_017010798.1:c.922A>C | XP_016866287.1:p.Ile308Leu | |
| NM_001384272.1:c.922A>C MANE Select | NP_001371201.1:p.Ile308Leu | |
| NM_001526.5:c.922A>C | NP_001517.2:p.Ile308Leu |