Revel Score:
ENST00000261304 (MANE Select)
0.029
ENST00000393568
0.029
ENST00000445021
0.029
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.87993137A>T , CM000676.2:g.87993137A>T | GRCh38 |
| NC_000014.8:g.88459481A>T , CM000676.1:g.88459481A>T | GRCh37 |
| NC_000014.7:g.87529234A>T | NCBI36 |
| NG_011853.2:g.5427T>A | |
| NG_011853.3:g.5427T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261304.7:c.28T>A MANE Select | ENSP00000261304.2:p.Trp10Arg | |
| ENST00000261304.6:c.28T>A | ENSP00000261304.2:p.Trp10Arg | |
| ENST00000393568.8:c.28T>A | ENSP00000377198.4:p.Trp10Arg | |
| ENST00000393569.6:c.117+246T>A | ENSP00000377199.2:n.117+246T>A | |
| ENST00000474294.6:n.18T>A | ||
| ENST00000554372.5:c.28T>A | ENSP00000451884.1:p.Trp10Arg | |
| ENST00000557316.5:c.28T>A | ENSP00000452314.1:p.Trp10Arg | |
| ENST00000622264.4:c.18T>A | ||
| NM_000153.3:c.28T>A | NP_000144.2:p.Trp10Arg | |
| NM_001201401.1:c.28T>A | NP_001188330.1:p.Trp10Arg | |
| NM_001201402.1:c.117+246T>A | NP_001188331.1:n.117+246T>A | |
| NM_000153.4:c.28T>A MANE Select | NP_000144.2:p.Trp10Arg | |
| NM_001201401.2:c.28T>A | NP_001188330.1:p.Trp10Arg | |
| NM_001201402.2:c.117+246T>A | NP_001188331.1:n.117+246T>A |