Revel Score:
ENST00000388922 (MANE Select)
0.914
ENST00000267008
0.914
ENST00000550683
0.914
ENST00000548659
0.914
ENST00000419526
0.914
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.51920843A>C , CM000674.2:g.51920843A>C | GRCh38 |
| NC_000012.11:g.52314627A>C , CM000674.1:g.52314627A>C | GRCh37 |
| NC_000012.10:g.50600894A>C | NCBI36 |
| NG_009549.1:g.18426A>C , LRG_543:g.18426A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000547400.6:c.1192A>C | ENSP00000446724.2:p.Thr398Pro | |
| ENST00000551576.6:c.1462A>C | ENSP00000455848.2:p.Thr488Pro | |
| ENST00000388922.9:c.1462A>C MANE Select | ENSP00000373574.4:p.Thr488Pro | |
| ENST00000388922.8:c.1462A>C | ENSP00000373574.4:p.Thr488Pro | |
| ENST00000419526.6:c.940A>C | ENSP00000392492.2:p.Thr314Pro | |
| ENST00000550683.5:c.1504A>C | ENSP00000447884.1:p.Thr502Pro | |
| NM_000020.2:c.1462A>C , LRG_543t1:c.1462A>C | NP_000011.2:p.Thr488Pro | |
| NM_001077401.1:c.1462A>C | NP_001070869.1:p.Thr488Pro | |
| XM_005269235.2:c.1462A>C | XP_005269292.1:p.Thr488Pro | |
| XM_011539008.1:c.1192A>C | XP_011537310.1:p.Thr398Pro | |
| XM_024449279.1:c.673A>C | XP_024305047.1:p.Thr225Pro | |
| NM_000020.3:c.1462A>C MANE Select | NP_000011.2:p.Thr488Pro | |
| NM_001077401.2:c.1462A>C | NP_001070869.1:p.Thr488Pro |