Revel Score:
ENST00000205557 (MANE Select)
0.899
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.16177623G>C , CM000678.2:g.16177623G>C | GRCh38 |
| NC_000016.9:g.16271480G>C , CM000678.1:g.16271480G>C | GRCh37 |
| NC_000016.8:g.16178981G>C | NCBI36 |
| NG_007558.2:g.50849C>G | |
| NG_007558.3:g.50995C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622290.5:c.2419C>G | ENSP00000483331.2:p.Arg807Gly | |
| ENST00000205557.12:c.2419C>G MANE Select | ENSP00000205557.7:p.Arg807Gly | |
| ENST00000205557.11:c.2419C>G | ENSP00000205557.7:p.Arg807Gly | |
| ENST00000456970.6:c.2415+1175C>G | ENSP00000405002.2:n.2415+1175C>G | |
| ENST00000622290.4:c.2415+1175C>G | ENSP00000483331.1:n.2415+1175C>G | |
| NM_001171.5:c.2419C>G | NP_001162.4:p.Arg807Gly | |
| XM_011522479.1:c.2386C>G | XP_011520781.1:p.Arg796Gly | |
| XM_011522480.1:c.2077C>G | XP_011520782.1:p.Arg693Gly | |
| XM_011522481.1:c.2077C>G | XP_011520783.1:p.Arg693Gly | |
| XM_011522482.1:c.2419C>G | XP_011520784.1:p.Arg807Gly | |
| XR_932836.1:n.2654C>G | ||
| XR_932837.1:n.2655C>G | ||
| XR_932838.1:n.2655C>G | ||
| NM_001351800.1:c.2077C>G | NP_001338729.1:p.Arg693Gly | |
| NR_147784.1:n.2452+1175C>G | ||
| XM_011522479.2:c.2386C>G | XP_011520781.1:p.Arg796Gly | |
| XM_011522481.3:c.2077C>G | XP_011520783.1:p.Arg693Gly | |
| XM_011522482.3:c.2419C>G | XP_011520784.1:p.Arg807Gly | |
| XM_017023212.1:c.2251C>G | XP_016878701.1:p.Arg751Gly | |
| XM_017023214.1:c.2419C>G | XP_016878703.1:p.Arg807Gly | |
| XM_024450261.1:c.2455C>G | XP_024306029.1:p.Arg819Gly | |
| XR_932836.2:n.2600C>G | ||
| XR_932837.3:n.2600C>G | ||
| XR_932838.3:n.2600C>G | ||
| NM_001171.6:c.2419C>G MANE Select | NP_001162.5:p.Arg807Gly |