Revel Score:
ENST00000155840 (MANE Select)
0.986
ENST00000335475
0.986
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2583447A>C , CM000673.2:g.2583447A>C | GRCh38 |
| NC_000011.9:g.2604677A>C , CM000673.1:g.2604677A>C | GRCh37 |
| NC_000011.8:g.2561253A>C | NCBI36 |
| NG_008935.1:g.143457A>C , LRG_287:g.143457A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496887.7:c.673A>C | ENSP00000434560.2:p.Thr225Pro | |
| ENST00000646564.2:c.490A>C | ENSP00000495806.2:p.Thr164Pro | |
| ENST00000155840.12:c.934A>C MANE Select | ENSP00000155840.2:p.Thr312Pro | |
| ENST00000335475.6:c.553A>C | ENSP00000334497.5:p.Thr185Pro | |
| ENST00000646564.1:c.136A>C | ENSP00000495806.1:p.Thr46Pro | |
| ENST00000155840.9:c.934A>C | ENSP00000155840.2:p.Thr312Pro | |
| ENST00000335475.5:c.553A>C | ENSP00000334497.5:p.Thr185Pro | |
| NM_000218.2:c.934A>C , LRG_287t1:c.934A>C | NP_000209.2:p.Thr312Pro | |
| NM_181798.1:c.553A>C , LRG_287t2:c.553A>C | NP_861463.1:p.Thr185Pro | |
| NM_000218.3:c.934A>C MANE Select | NP_000209.2:p.Thr312Pro |