Revel Score:
ENST00000310926 (MANE Select)
0.901
ENST00000493729
0.901
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.133973750C>G , CM000665.2:g.133973750C>G | GRCh38 |
| NC_000003.11:g.133692594C>G , CM000665.1:g.133692594C>G | GRCh37 |
| NC_000003.10:g.135175284C>G | NCBI36 |
| NG_031964.2:g.83435G>C | |
| NG_031964.3:g.83435G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310926.11:c.310G>C MANE Select | ENSP00000311291.4:p.Gly104Arg | |
| ENST00000310926.8:c.310G>C | ENSP00000311291.4:p.Gly104Arg | |
| ENST00000462770.5:n.433G>C | ||
| ENST00000464676.5:n.572G>C | ||
| ENST00000478651.1:n.433G>C | ||
| ENST00000481359.3:c.310G>C | ENSP00000420028.3:p.Gly104Arg | |
| ENST00000493729.5:c.310G>C | ENSP00000418893.1:p.Gly104Arg | |
| NM_005630.2:c.310G>C | NP_005621.2:p.Gly104Arg | |
| XM_011513090.1:c.310G>C | XP_011511392.1:p.Gly104Arg | |
| XM_017007077.1:c.-195G>C | XP_016862566.1:n.-195G>C | |
| XM_024453721.1:c.310G>C | XP_024309489.1:p.Gly104Arg | |
| NM_005630.3:c.310G>C MANE Select | NP_005621.2:p.Gly104Arg |