Revel Score:
ENST00000297268 (MANE Select)
0.941
ENST00000545487
0.941
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94410501G>A , CM000669.2:g.94410501G>A | GRCh38 |
| NC_000007.13:g.94039813G>A , CM000669.1:g.94039813G>A | GRCh37 |
| NC_000007.12:g.93877749G>A | NCBI36 |
| NG_007405.1:g.20941G>A , LRG_2:g.20941G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.1171G>A MANE Select | ENSP00000297268.6:p.Gly391Ser | |
| ENST00000297268.10:c.1171G>A | ENSP00000297268.6:p.Gly391Ser | |
| ENST00000620463.1:c.1165G>A | ENSP00000477719.1:p.Gly389Ser | |
| NM_000089.3:c.1171G>A , LRG_2t1:c.1171G>A | NP_000080.2:p.Gly391Ser | |
| NM_000089.4:c.1171G>A MANE Select | NP_000080.2:p.Gly391Ser |