Revel Score:
ENST00000300527 (MANE Select)
0.982
ENST00000357838
0.982
ENST00000310645
0.982
ENST00000409416
0.982
ENST00000397763 (MANE Plus Clinical)
0.982
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.46115882G>T , CM000683.2:g.46115882G>T | GRCh38 |
| NC_000021.8:g.47535796G>T , CM000683.1:g.47535796G>T | GRCh37 |
| NC_000021.7:g.46360224G>T | NCBI36 |
| NG_008675.1:g.22764G>T , LRG_476:g.22764G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397763.6:c.812G>T MANE Plus Clinical | ENSP00000380870.1:p.Gly271Val | |
| ENST00000300527.9:c.812G>T MANE Select | ENSP00000300527.4:p.Gly271Val | |
| ENST00000409416.6:c.812G>T | ENSP00000387115.1:p.Gly271Val | |
| ENST00000300527.8:c.812G>T | ENSP00000300527.4:p.Gly271Val | |
| ENST00000310645.9:c.812G>T | ENSP00000312529.5:p.Gly271Val | |
| ENST00000397763.5:c.812G>T | ENSP00000380870.1:p.Gly271Val | |
| ENST00000409416.5:c.812G>T | ENSP00000387115.1:p.Gly271Val | |
| ENST00000485591.1:n.468G>T | ||
| NM_001849.3:c.812G>T , LRG_476t1:c.812G>T | NP_001840.3:p.Gly271Val | |
| NM_058174.2:c.812G>T | NP_478054.2:p.Gly271Val | |
| NM_058175.2:c.812G>T | NP_478055.2:p.Gly271Val | |
| XM_011529451.1:c.812G>T | XP_011527753.1:p.Gly271Val | |
| XM_011529452.1:c.812G>T | XP_011527754.1:p.Gly271Val | |
| XR_937438.1:n.935G>T | ||
| XR_937439.1:n.935G>T | ||
| XR_937438.2:n.942G>T | ||
| XR_937439.2:n.942G>T | ||
| NM_001849.4:c.812G>T MANE Select | NP_001840.3:p.Gly271Val | |
| NM_058174.3:c.812G>T MANE Plus Clinical | NP_478054.2:p.Gly271Val | |
| NM_058175.3:c.812G>T | NP_478055.2:p.Gly271Val |