Revel Score:
ENST00000297268 (MANE Select)
0.912
ENST00000545487
0.912
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94426514G>C , CM000669.2:g.94426514G>C | GRCh38 |
| NC_000007.13:g.94055826G>C , CM000669.1:g.94055826G>C | GRCh37 |
| NC_000007.12:g.93893762G>C | NCBI36 |
| NG_007405.1:g.36954G>C , LRG_2:g.36954G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.3089G>C MANE Select | ENSP00000297268.6:p.Gly1030Ala | |
| ENST00000297268.10:c.3089G>C | ENSP00000297268.6:p.Gly1030Ala | |
| ENST00000478215.1:n.648G>C | ||
| ENST00000481570.5:n.3062G>C | ||
| ENST00000488121.1:n.5G>C | ||
| ENST00000620463.1:c.3083G>C | ENSP00000477719.1:p.Gly1028Ala | |
| NM_000089.3:c.3089G>C , LRG_2t1:c.3089G>C | NP_000080.2:p.Gly1030Ala | |
| NM_000089.4:c.3089G>C MANE Select | NP_000080.2:p.Gly1030Ala |