Revel Score:
ENST00000218032 (MANE Select)
0.215
ENST00000311912
0.215
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.12920520T>C , CM000685.2:g.12920520T>C | GRCh38 |
| NC_000023.10:g.12938639T>C , CM000685.1:g.12938639T>C | GRCh37 |
| NC_000023.9:g.12848560T>C | NCBI36 |
| NG_012882.2:g.18901T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218032.7:c.1480T>C (TLR8) MANE Select | ENSP00000218032.7:p.Phe494Leu | |
| ENST00000218032.6:c.1480T>C (TLR8) | ENSP00000218032.6:p.Phe494Leu | |
| ENST00000311912.5:c.1534T>C (TLR8) | ENSP00000312082.5:p.Phe512Leu | |
| NM_016610.3:c.1534T>C (TLR8) | NP_057694.2:p.Phe512Leu | |
| NM_138636.5:c.1480T>C (TLR8) MANE Select | NP_619542.1:p.Phe494Leu | |
| NR_030727.1:n.241-12187A>G (TLR8-AS1) | ||
| XM_011545529.1:c.1534T>C (TLR8) | XP_011543831.1:p.Phe512Leu | |
| XM_011545530.1:c.1534T>C (TLR8) | XP_011543832.1:p.Phe512Leu | |
| XM_011545530.2:c.1534T>C (TLR8) | XP_011543832.1:p.Phe512Leu | |
| NM_016610.4:c.1534T>C (TLR8) | NP_057694.2:p.Phe512Leu |