Revel Score:
ENST00000388922 (MANE Select)
0.765
ENST00000267008
0.765
ENST00000550683
0.765
ENST00000548659
0.765
ENST00000419526
0.765
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.51919008C>T , CM000674.2:g.51919008C>T | GRCh38 |
| NC_000012.11:g.52312792C>T , CM000674.1:g.52312792C>T | GRCh37 |
| NC_000012.10:g.50599059C>T | NCBI36 |
| NG_009549.1:g.16591C>T , LRG_543:g.16591C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000547400.6:c.1000C>T | ENSP00000446724.2:p.Pro334Ser | |
| ENST00000551576.6:c.1270C>T | ENSP00000455848.2:p.Pro424Ser | |
| ENST00000552678.2:c.1270C>T | ENSP00000457394.2:p.Pro424Ser | |
| ENST00000388922.9:c.1270C>T MANE Select | ENSP00000373574.4:p.Pro424Ser | |
| ENST00000388922.8:c.1270C>T | ENSP00000373574.4:p.Pro424Ser | |
| ENST00000419526.6:c.748C>T | ENSP00000392492.2:p.Pro250Ser | |
| ENST00000547632.1:n.545C>T | ||
| ENST00000550683.5:c.1312C>T | ENSP00000447884.1:p.Pro438Ser | |
| ENST00000552678.1:c.275C>T | ||
| NM_000020.2:c.1270C>T , LRG_543t1:c.1270C>T | NP_000011.2:p.Pro424Ser | |
| NM_001077401.1:c.1270C>T | NP_001070869.1:p.Pro424Ser | |
| XM_005269235.2:c.1270C>T | XP_005269292.1:p.Pro424Ser | |
| XM_011539008.1:c.1000C>T | XP_011537310.1:p.Pro334Ser | |
| XM_024449279.1:c.481C>T | XP_024305047.1:p.Pro161Ser | |
| NM_000020.3:c.1270C>T MANE Select | NP_000011.2:p.Pro424Ser | |
| NM_001077401.2:c.1270C>T | NP_001070869.1:p.Pro424Ser |