Revel Score:
ENST00000340941 (MANE Select)
0.956
ENST00000323375
0.956
ENST00000509539
0.956
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.71646220T>C , CM000667.2:g.71646220T>C | GRCh38 |
| NC_000005.9:g.70942047T>C , CM000667.1:g.70942047T>C | GRCh37 |
| NC_000005.8:g.70977803T>C | NCBI36 |
| NG_008882.1:g.63933T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000505435.4:n.2767T>C | ||
| ENST00000505787.8:n.2990T>C | ||
| ENST00000509539.3:c.485T>C | ENSP00000425474.3:n.485T>C | |
| ENST00000681968.1:c.652T>C | ENSP00000508143.1:p.Phe218Leu | |
| ENST00000681991.1:n.1243T>C | ||
| ENST00000682045.1:c.1015T>C | ENSP00000507329.1:p.Phe339Leu | |
| ENST00000682214.1:c.766T>C | ENSP00000507336.1:p.Phe256Leu | |
| ENST00000682231.1:n.177T>C | ||
| ENST00000682438.1:n.3158T>C | ||
| ENST00000682499.1:n.1980T>C | ||
| ENST00000682541.1:c.*57T>C | ENSP00000507673.1:n.*57T>C | |
| ENST00000682640.1:n.863T>C | ||
| ENST00000682667.1:n.1324T>C | ||
| ENST00000682687.1:c.*111T>C | ENSP00000507945.1:n.*111T>C | |
| ENST00000682727.1:c.1150T>C | ENSP00000507393.1:p.Phe384Leu | |
| ENST00000682876.1:c.1288T>C | ENSP00000508389.1:p.Phe430Leu | |
| ENST00000683098.1:c.813T>C | ENSP00000507670.1:p.Thr271= | |
| ENST00000683258.1:c.*880T>C | ENSP00000507448.1:n.*880T>C | |
| ENST00000683339.1:c.943T>C | ENSP00000507758.1:p.Phe315Leu | |
| ENST00000683403.1:c.1069T>C | ENSP00000507896.1:p.Phe357Leu | |
| ENST00000683429.1:c.766T>C | ENSP00000507697.1:p.Phe256Leu | |
| ENST00000683789.1:c.1045T>C | ENSP00000507012.1:p.Phe349Leu | |
| ENST00000683847.1:n.1329T>C | ||
| ENST00000683882.1:c.*100T>C | ENSP00000506735.1:n.*100T>C | |
| ENST00000684024.1:c.*830T>C | ENSP00000507175.1:n.*830T>C | |
| ENST00000684132.1:c.87T>C | ||
| ENST00000684254.1:c.*885T>C | ENSP00000508001.1:n.*885T>C | |
| ENST00000684310.1:c.325T>C | ENSP00000507550.1:p.Phe109Leu | |
| ENST00000684474.1:n.795T>C | ||
| ENST00000684530.1:c.335-2877T>C | ENSP00000507439.1:n.335-2877T>C | |
| ENST00000684686.1:n.778T>C | ||
| ENST00000340941.11:c.1159T>C MANE Select | ENSP00000343657.6:p.Phe387Leu | |
| ENST00000340941.10:c.1159T>C | ENSP00000343657.6:p.Phe387Leu | |
| ENST00000509539.2:c.475T>C | ENSP00000425474.2:p.Phe159Leu | |
| ENST00000512218.6:c.*111T>C | ENSP00000423202.2:n.*111T>C | |
| NM_022132.4:c.1159T>C | NP_071415.1:p.Phe387Leu | |
| XM_005248567.1:c.1045T>C | XP_005248624.1:p.Phe349Leu | |
| NM_001363147.1:c.1045T>C | NP_001350076.1:p.Phe349Leu | |
| XR_001742172.1:n.1247T>C | ||
| NM_022132.5:c.1159T>C MANE Select | NP_071415.1:p.Phe387Leu |