Revel Score:
ENST00000205557 (MANE Select)
0.332
ENST00000205558
0.332
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.16159541G>C , CM000678.2:g.16159541G>C | GRCh38 |
| NC_000016.9:g.16253398G>C , CM000678.1:g.16253398G>C | GRCh37 |
| NC_000016.8:g.16160899G>C | NCBI36 |
| NG_007558.2:g.68931C>G | |
| NG_007558.3:g.69077C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622290.5:c.3676C>G | ENSP00000483331.2:p.Leu1226Val | |
| ENST00000205557.12:c.3676C>G MANE Select | ENSP00000205557.7:p.Leu1226Val | |
| ENST00000640696.1:c.490C>G | ENSP00000492197.1:p.Leu164Val | |
| ENST00000205557.11:c.3676C>G | ENSP00000205557.7:p.Leu1226Val | |
| ENST00000456970.6:c.3301C>G | ENSP00000405002.2:n.3301C>G | |
| ENST00000622290.4:c.*885C>G | ENSP00000483331.1:n.*885C>G | |
| NM_001171.5:c.3676C>G | NP_001162.4:p.Leu1226Val | |
| XM_011522479.1:c.3643C>G | XP_011520781.1:p.Leu1215Val | |
| XM_011522480.1:c.3334C>G | XP_011520782.1:p.Leu1112Val | |
| XM_011522481.1:c.3334C>G | XP_011520783.1:p.Leu1112Val | |
| XR_932836.1:n.3911C>G | ||
| XR_932837.1:n.3712C>G | ||
| XR_932838.1:n.3712C>G | ||
| XR_933134.1:n.539-240G>C | ||
| NM_001351800.1:c.3334C>G | NP_001338729.1:p.Leu1112Val | |
| NR_147784.1:n.3338C>G | ||
| XM_011522479.2:c.3643C>G | XP_011520781.1:p.Leu1215Val | |
| XM_011522481.3:c.3334C>G | XP_011520783.1:p.Leu1112Val | |
| XM_017023212.1:c.3508C>G | XP_016878701.1:p.Leu1170Val | |
| XM_024450261.1:c.3712C>G | XP_024306029.1:p.Leu1238Val | |
| XR_932836.2:n.3857C>G | ||
| XR_932837.3:n.3657C>G | ||
| XR_932838.3:n.3657C>G | ||
| NM_001171.6:c.3676C>G MANE Select | NP_001162.5:p.Leu1226Val |