Revel Score:
ENST00000557233
0.252
ENST00000293826
0.252
ENST00000438470
0.252
ENST00000436057
0.252
ENST00000349228
0.252
ENST00000338784 (MANE Select)
0.252
ENST00000396545
0.252
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7559652A>T , CM000679.2:g.7559652A>T | GRCh38 |
| NC_000017.10:g.7462969A>T , CM000679.1:g.7462969A>T | GRCh37 |
| NC_000017.9:g.7403693A>T | NCBI36 |
| NG_029949.1:g.6361A>T | |
| NG_052944.1:g.15595A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338784.9:c.287A>T (TNFSF13) MANE Select | ENSP00000343505.4:p.Asn96Ile | |
| ENST00000293826.4:c.527A>T (TNFSF12-TNFSF13) | ENSP00000293826.4:p.Asn176Ile | |
| ENST00000338784.8:c.287A>T (TNFSF13) | ENSP00000343505.4:p.Asn96Ile | |
| ENST00000349228.8:c.287A>T (TNFSF13) | ENSP00000314455.6:p.Asn96Ile | |
| ENST00000380535.8:c.259-196A>T (TNFSF13) | ENSP00000369908.5:n.259-196A>T | |
| ENST00000396542.5:c.208-199A>T (TNFSF13) | ENSP00000379792.1:n.208-199A>T | |
| ENST00000396545.4:c.287A>T (TNFSF13) | ENSP00000379794.4:p.Asn96Ile | |
| ENST00000436057.5:c.236A>T (TNFSF13) | ENSP00000410094.1:p.Asn79Ile | |
| ENST00000438470.5:c.236A>T (TNFSF13) | ENSP00000390771.1:p.Asn79Ile | |
| ENST00000483039.5:c.-71-194A>T (TNFSF13) | ENSP00000464998.1:n.-71-194A>T | |
| ENST00000625791.2:c.259-199A>T (TNFSF13) | ENSP00000486052.1:n.259-199A>T | |
| NM_001198622.1:c.259-196A>T (TNFSF13) | NP_001185551.1:n.259-196A>T | |
| NM_001198623.1:c.259-199A>T (TNFSF13) | NP_001185552.1:n.259-199A>T | |
| NM_001198624.1:c.208-199A>T (TNFSF13) | NP_001185553.1:n.208-199A>T | |
| NM_003808.3:c.287A>T (TNFSF13) | NP_003799.1:p.Asn96Ile | |
| NM_172087.2:c.287A>T (TNFSF13) | NP_742084.1:p.Asn96Ile | |
| NM_172088.2:c.287A>T (TNFSF13) | NP_742085.1:p.Asn96Ile | |
| NM_172089.3:c.527A>T (TNFSF12-TNFSF13) | NP_742086.1:p.Asn176Ile | |
| NR_073490.2:n.1006+355A>T (TNFSF13) | ||
| NM_172089.4:c.527A>T (TNFSF12-TNFSF13) | NP_742086.1:p.Asn176Ile | |
| NM_001198622.2:c.259-196A>T (TNFSF13) | NP_001185551.1:n.259-196A>T | |
| NM_001198623.2:c.259-199A>T (TNFSF13) | NP_001185552.1:n.259-199A>T | |
| NM_001198624.2:c.208-199A>T (TNFSF13) | NP_001185553.1:n.208-199A>T | |
| NM_003808.4:c.287A>T (TNFSF13) MANE Select | NP_003799.1:p.Asn96Ile | |
| NM_172087.3:c.287A>T (TNFSF13) | NP_742084.1:p.Asn96Ile | |
| NM_172088.4:c.287A>T (TNFSF13) | NP_742085.1:p.Asn96Ile | |
| NR_073490.3:n.548+355A>T (TNFSF13) |