Revel Score:
ENST00000218032 (MANE Select)
0.441
ENST00000311912
0.441
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.12920755G>T , CM000685.2:g.12920755G>T | GRCh38 |
| NC_000023.10:g.12938874G>T , CM000685.1:g.12938874G>T | GRCh37 |
| NC_000023.9:g.12848795G>T | NCBI36 |
| NG_012882.2:g.19136G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218032.7:c.1715G>T (TLR8) MANE Select | ENSP00000218032.7:p.Gly572Val | |
| ENST00000218032.6:c.1715G>T (TLR8) | ENSP00000218032.6:p.Gly572Val | |
| ENST00000311912.5:c.1769G>T (TLR8) | ENSP00000312082.5:p.Gly590Val | |
| NM_016610.3:c.1769G>T (TLR8) | NP_057694.2:p.Gly590Val | |
| NM_138636.5:c.1715G>T (TLR8) MANE Select | NP_619542.1:p.Gly572Val | |
| NR_030727.1:n.241-12422C>A (TLR8-AS1) | ||
| XM_011545529.1:c.1769G>T (TLR8) | XP_011543831.1:p.Gly590Val | |
| XM_011545530.1:c.1769G>T (TLR8) | XP_011543832.1:p.Gly590Val | |
| XM_011545530.2:c.1769G>T (TLR8) | XP_011543832.1:p.Gly590Val | |
| NM_016610.4:c.1769G>T (TLR8) | NP_057694.2:p.Gly590Val |