Revel Score:
ENST00000294304 (MANE Select)
0.664
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.68423568G>C , CM000673.2:g.68423568G>C | GRCh38 |
| NC_000011.9:g.68191036G>C , CM000673.1:g.68191036G>C | GRCh37 |
| NC_000011.8:g.67947612G>C | NCBI36 |
| NG_015835.1:g.115929G>C | |
| NG_015835.2:g.115929G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000294304.12:c.3107G>C MANE Select | ENSP00000294304.6:p.Arg1036Pro | |
| ENST00000294304.11:c.3107G>C | ENSP00000294304.6:p.Arg1036Pro | |
| ENST00000529993.5:c.*1713G>C | ENSP00000436652.1:n.*1713G>C | |
| NM_001291902.1:c.1364G>C | NP_001278831.1:p.Arg455Pro | |
| NM_002335.3:c.3107G>C | NP_002326.2:p.Arg1036Pro | |
| XM_005273994.2:c.3107G>C | XP_005274051.1:p.Arg1036Pro | |
| XM_011545029.1:c.3134G>C | XP_011543331.1:p.Arg1045Pro | |
| XM_011545030.1:c.3134G>C | XP_011543332.1:p.Arg1045Pro | |
| XM_011545031.1:c.3134G>C | XP_011543333.1:p.Arg1045Pro | |
| XR_949925.1:n.3149G>C | ||
| XR_949926.1:n.3149G>C | ||
| XM_017017735.1:c.1364G>C | XP_016873224.1:p.Arg455Pro | |
| XM_017017736.1:c.647G>C | XP_016873225.1:p.Arg216Pro | |
| XR_949925.2:n.3149G>C | ||
| XR_949926.2:n.3149G>C | ||
| NM_002335.4:c.3107G>C MANE Select | NP_002326.2:p.Arg1036Pro | |
| NM_001291902.2:c.1364G>C | NP_001278831.1:p.Arg455Pro |