Revel Score:
ENST00000298296 (MANE Select)
0.029
ENST00000448920
0.029
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.141895341G>C , CM000685.2:g.141895341G>C | GRCh38 |
| NC_000023.10:g.140983127G>C , CM000685.1:g.140983127G>C | GRCh37 |
| NC_000023.9:g.140810793G>C | NCBI36 |
| NG_013272.1:g.62026G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000298296.1:c.982G>C MANE Select | ENSP00000298296.1:p.Ala328Pro | |
| ENST00000443323.2:c.-118-1090G>C | ENSP00000438254.1:n.-118-1090G>C | |
| ENST00000483584.5:n.222G>C | ||
| ENST00000544766.5:c.-306G>C | ENSP00000440444.1:n.-306G>C | |
| NM_138702.1:c.982G>C MANE Select | NP_619647.1:p.Ala328Pro | |
| NM_177456.2:c.-306G>C | NP_803251.1:n.-306G>C | |
| XM_011531267.1:c.-229G>C | XP_011529569.1:n.-229G>C | |
| XM_011531267.3:c.-229G>C | XP_011529569.1:n.-229G>C | |
| XM_017029265.2:c.-306G>C | XP_016884754.1:n.-306G>C |