Revel Score:
ENST00000268251 (MANE Select)
0.942
ENST00000396600
0.942
ENST00000425191
0.942
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.8781360T>A , CM000678.2:g.8781360T>A | GRCh38 |
| NC_000016.9:g.8875217T>A , CM000678.1:g.8875217T>A | GRCh37 |
| NC_000016.8:g.8782718T>A | NCBI36 |
| NG_008432.1:g.111774T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268251.13:c.1433T>A (ABAT) MANE Select | ENSP00000268251.8:p.Leu478Gln | |
| ENST00000268251.12:c.1433T>A (ABAT) | ENSP00000268251.8:p.Leu478Gln | |
| ENST00000396600.6:c.1433T>A (ABAT) | ENSP00000379845.2:p.Leu478Gln | |
| ENST00000425191.6:c.1433T>A (ABAT) | ENSP00000411916.2:p.Leu478Gln | |
| ENST00000564869.1:n.116A>T (TMEM186) | ||
| ENST00000566590.5:c.*1173T>A (ABAT) | ENSP00000455198.1:n.*1173T>A | |
| ENST00000567812.5:c.1478T>A (ABAT) | ENSP00000456330.1:p.Leu493Gln | |
| ENST00000569156.5:c.1492T>A (ABAT) | ENSP00000454963.1:p.Trp498Arg | |
| NM_000663.4:c.1433T>A (ABAT) | NP_000654.2:p.Leu478Gln | |
| NM_001127448.1:c.1433T>A (ABAT) | NP_001120920.1:p.Leu478Gln | |
| NM_020686.5:c.1433T>A (ABAT) | NP_065737.2:p.Leu478Gln | |
| XM_011522400.1:c.1433T>A (ABAT) | XP_011520702.1:p.Leu478Gln | |
| XM_011522401.1:c.1433T>A (ABAT) | XP_011520703.1:p.Leu478Gln | |
| XM_011522400.2:c.1433T>A (ABAT) | XP_011520702.1:p.Leu478Gln | |
| XM_011522401.2:c.1433T>A (ABAT) | XP_011520703.1:p.Leu478Gln | |
| NM_020686.6:c.1433T>A (ABAT) MANE Select | NP_065737.2:p.Leu478Gln | |
| NM_001127448.2:c.1433T>A (ABAT) | NP_001120920.1:p.Leu478Gln | |
| NM_000663.5:c.1433T>A (ABAT) | NP_000654.2:p.Leu478Gln | |
| NM_001386600.1:c.1433T>A (ABAT) | NP_001373529.1:p.Leu478Gln | |
| NM_001386601.1:c.1433T>A (ABAT) | NP_001373530.1:p.Leu478Gln | |
| NM_001386602.1:c.1433T>A (ABAT) | NP_001373531.1:p.Leu478Gln | |
| NM_001386603.1:c.1433T>A (ABAT) | NP_001373532.1:p.Leu478Gln | |
| NM_001386604.1:c.1433T>A (ABAT) | NP_001373533.1:p.Leu478Gln | |
| NM_001386605.1:c.1394T>A (ABAT) | NP_001373534.1:p.Leu465Gln | |
| NM_001386606.1:c.1370T>A (ABAT) | NP_001373535.1:p.Leu457Gln | |
| NM_001386607.1:c.1370T>A (ABAT) | NP_001373536.1:p.Leu457Gln | |
| NM_001386608.1:c.1340T>A (ABAT) | NP_001373537.1:p.Leu447Gln | |
| NM_001386609.1:c.1321T>A (ABAT) | NP_001373538.1:p.Trp441Arg | |
| NM_001386610.1:c.1298T>A (ABAT) | NP_001373539.1:p.Leu433Gln | |
| NM_001386611.1:c.1298T>A (ABAT) | NP_001373540.1:p.Leu433Gln | |
| NM_001386612.1:c.1235T>A (ABAT) | NP_001373541.1:p.Leu412Gln | |
| NM_001386613.1:c.1235T>A (ABAT) | NP_001373542.1:p.Leu412Gln | |
| NM_001386614.1:c.1187T>A (ABAT) | NP_001373543.1:p.Leu396Gln | |
| NM_001386615.1:c.1529T>A (ABAT) | NP_001373544.1:p.Leu510Gln | |
| NM_001386616.1:c.1492T>A (ABAT) | NP_001373545.1:p.Trp498Arg |