Revel Score:
ENST00000388922 (MANE Select)
0.931
ENST00000267008
0.931
ENST00000550683
0.931
ENST00000548659
0.931
ENST00000419526
0.931
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.51920835T>C , CM000674.2:g.51920835T>C | GRCh38 |
| NC_000012.11:g.52314619T>C , CM000674.1:g.52314619T>C | GRCh37 |
| NC_000012.10:g.50600886T>C | NCBI36 |
| NG_009549.1:g.18418T>C , LRG_543:g.18418T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000547400.6:c.1184T>C | ENSP00000446724.2:p.Ile395Thr | |
| ENST00000551576.6:c.1454T>C | ENSP00000455848.2:p.Ile485Thr | |
| ENST00000388922.9:c.1454T>C MANE Select | ENSP00000373574.4:p.Ile485Thr | |
| ENST00000388922.8:c.1454T>C | ENSP00000373574.4:p.Ile485Thr | |
| ENST00000419526.6:c.932T>C | ENSP00000392492.2:p.Ile311Thr | |
| ENST00000550683.5:c.1496T>C | ENSP00000447884.1:p.Ile499Thr | |
| NM_000020.2:c.1454T>C , LRG_543t1:c.1454T>C | NP_000011.2:p.Ile485Thr | |
| NM_001077401.1:c.1454T>C | NP_001070869.1:p.Ile485Thr | |
| XM_005269235.2:c.1454T>C | XP_005269292.1:p.Ile485Thr | |
| XM_011539008.1:c.1184T>C | XP_011537310.1:p.Ile395Thr | |
| XM_024449279.1:c.665T>C | XP_024305047.1:p.Ile222Thr | |
| NM_000020.3:c.1454T>C MANE Select | NP_000011.2:p.Ile485Thr | |
| NM_001077401.2:c.1454T>C | NP_001070869.1:p.Ile485Thr |