Revel Score:
ENST00000205557 (MANE Select)
0.199
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.16173376G>C , CM000678.2:g.16173376G>C | GRCh38 |
| NC_000016.9:g.16267233G>C , CM000678.1:g.16267233G>C | GRCh37 |
| NC_000016.8:g.16174734G>C | NCBI36 |
| NG_007558.2:g.55096C>G | |
| NG_007558.3:g.55242C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622290.5:c.2695C>G | ENSP00000483331.2:p.Arg899Gly | |
| ENST00000205557.12:c.2695C>G MANE Select | ENSP00000205557.7:p.Arg899Gly | |
| ENST00000205557.11:c.2695C>G | ENSP00000205557.7:p.Arg899Gly | |
| ENST00000456970.6:c.2520C>G | ENSP00000405002.2:p.Thr840= | |
| ENST00000576683.1:n.182C>G | ||
| ENST00000622290.4:c.2520C>G | ENSP00000483331.1:p.Thr840= | |
| NM_001171.5:c.2695C>G | NP_001162.4:p.Arg899Gly | |
| XM_011522479.1:c.2662C>G | XP_011520781.1:p.Arg888Gly | |
| XM_011522480.1:c.2353C>G | XP_011520782.1:p.Arg785Gly | |
| XM_011522481.1:c.2353C>G | XP_011520783.1:p.Arg785Gly | |
| XM_011522482.1:c.*38C>G | XP_011520784.1:n.*38C>G | |
| XR_932836.1:n.2930C>G | ||
| XR_932837.1:n.2931C>G | ||
| XR_932838.1:n.2931C>G | ||
| NM_001351800.1:c.2353C>G | NP_001338729.1:p.Arg785Gly | |
| NR_147784.1:n.2557C>G | ||
| XM_011522479.2:c.2662C>G | XP_011520781.1:p.Arg888Gly | |
| XM_011522481.3:c.2353C>G | XP_011520783.1:p.Arg785Gly | |
| XM_011522482.3:c.*38C>G | XP_011520784.1:n.*38C>G | |
| XM_017023212.1:c.2527C>G | XP_016878701.1:p.Arg843Gly | |
| XM_017023214.1:c.2695C>G | XP_016878703.1:p.Arg899Gly | |
| XM_024450261.1:c.2731C>G | XP_024306029.1:p.Arg911Gly | |
| XR_932836.2:n.2876C>G | ||
| XR_932837.3:n.2876C>G | ||
| XR_932838.3:n.2876C>G | ||
| NM_001171.6:c.2695C>G MANE Select | NP_001162.5:p.Arg899Gly |