Revel Score:
ENST00000294304 (MANE Select)
0.943
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.68357802C>T , CM000673.2:g.68357802C>T | GRCh38 |
| NC_000011.9:g.68125270C>T , CM000673.1:g.68125270C>T | GRCh37 |
| NC_000011.8:g.67881846C>T | NCBI36 |
| NG_015835.1:g.50163C>T | |
| NG_015835.2:g.50163C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000294304.12:c.641C>T MANE Select | ENSP00000294304.6:p.Ala214Val | |
| ENST00000294304.11:c.641C>T | ENSP00000294304.6:p.Ala214Val | |
| ENST00000529993.5:c.641C>T | ENSP00000436652.1:p.Ala214Val | |
| NM_001291902.1:c.-1125C>T | NP_001278831.1:n.-1125C>T | |
| NM_002335.3:c.641C>T | NP_002326.2:p.Ala214Val | |
| XM_005273994.2:c.641C>T | XP_005274051.1:p.Ala214Val | |
| XM_011545029.1:c.668C>T | XP_011543331.1:p.Ala223Val | |
| XM_011545030.1:c.668C>T | XP_011543332.1:p.Ala223Val | |
| XM_011545031.1:c.668C>T | XP_011543333.1:p.Ala223Val | |
| XR_949925.1:n.683C>T | ||
| XR_949926.1:n.683C>T | ||
| XR_001747874.1:n.683C>T | ||
| XR_949925.2:n.683C>T | ||
| XR_949926.2:n.683C>T | ||
| NM_002335.4:c.641C>T MANE Select | NP_002326.2:p.Ala214Val | |
| NM_001291902.2:c.-1125C>T | NP_001278831.1:n.-1125C>T |