Revel Score:
ENST00000225964 (MANE Select)
0.962
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.50189009C>A , CM000679.2:g.50189009C>A | GRCh38 |
| NC_000017.10:g.48266370C>A , CM000679.1:g.48266370C>A | GRCh37 |
| NC_000017.9:g.45621369C>A | NCBI36 |
| NG_007400.1:g.17631G>T , LRG_1:g.17631G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225964.10:c.2939G>T MANE Select | ENSP00000225964.6:p.Gly980Val | |
| ENST00000225964.9:c.2939G>T | ENSP00000225964.5:p.Gly980Val | |
| NM_000088.3:c.2939G>T , LRG_1t1:c.2939G>T | NP_000079.2:p.Gly980Val | |
| XM_005257058.3:c.2669G>T | XP_005257115.2:p.Gly890Val | |
| XM_005257059.3:c.2021G>T | XP_005257116.2:p.Gly674Val | |
| XM_011524341.1:c.2741G>T | XP_011522643.1:p.Gly914Val | |
| XM_005257058.4:c.2669G>T | XP_005257115.2:p.Gly890Val | |
| XM_005257059.4:c.2021G>T | XP_005257116.2:p.Gly674Val | |
| NM_000088.4:c.2939G>T MANE Select | NP_000079.2:p.Gly980Val |