Revel Score:
ENST00000447527
0.776
ENST00000538123
0.993
ENST00000361216 (MANE Select)
0.993
ENST00000392233
0.993
ENST00000435866
0.993
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160128767C>T , CM000663.2:g.160128767C>T | GRCh38 |
| NC_000001.10:g.160098557C>T , CM000663.1:g.160098557C>T | GRCh37 |
| NC_000001.9:g.158365181C>T | NCBI36 |
| NG_008014.1:g.18010C>T , LRG_6:g.18010C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361216.8:c.1133C>T MANE Select | ENSP00000354490.3:p.Thr378Ile | |
| ENST00000361216.7:c.1133C>T | ENSP00000354490.3:p.Thr378Ile | |
| ENST00000392233.7:c.1133C>T | ENSP00000376066.3:p.Thr378Ile | |
| ENST00000447527.1:c.265C>T | ||
| ENST00000472488.5:n.1236C>T | ||
| NM_000702.3:c.1133C>T | NP_000693.1:p.Thr378Ile | |
| NM_000702.4:c.1133C>T MANE Select | NP_000693.1:p.Thr378Ile |