Revel Score:
ENST00000297268 (MANE Select)
0.969
ENST00000545487
0.969
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94414258G>A , CM000669.2:g.94414258G>A | GRCh38 |
| NC_000007.13:g.94043570G>A , CM000669.1:g.94043570G>A | GRCh37 |
| NC_000007.12:g.93881506G>A | NCBI36 |
| NG_007405.1:g.24698G>A , LRG_2:g.24698G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.1702G>A MANE Select | ENSP00000297268.6:p.Gly568Ser | |
| ENST00000297268.10:c.1702G>A | ENSP00000297268.6:p.Gly568Ser | |
| ENST00000473573.5:n.39G>A | ||
| ENST00000488298.5:n.126G>A | ||
| ENST00000620463.1:c.1696G>A | ENSP00000477719.1:p.Gly566Ser | |
| NM_000089.3:c.1702G>A , LRG_2t1:c.1702G>A | NP_000080.2:p.Gly568Ser | |
| NM_000089.4:c.1702G>A MANE Select | NP_000080.2:p.Gly568Ser |