Revel Score:
ENST00000340941 (MANE Select)
0.967
ENST00000323375
0.967
ENST00000509539
0.967
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.71646221T>C , CM000667.2:g.71646221T>C | GRCh38 |
| NC_000005.9:g.70942048T>C , CM000667.1:g.70942048T>C | GRCh37 |
| NC_000005.8:g.70977804T>C | NCBI36 |
| NG_008882.1:g.63934T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000505435.4:n.2768T>C | ||
| ENST00000505787.8:n.2991T>C | ||
| ENST00000509539.3:c.486T>C | ENSP00000425474.3:n.486T>C | |
| ENST00000681968.1:c.653T>C | ENSP00000508143.1:p.Phe218Ser | |
| ENST00000681991.1:n.1244T>C | ||
| ENST00000682045.1:c.1016T>C | ENSP00000507329.1:p.Phe339Ser | |
| ENST00000682214.1:c.767T>C | ENSP00000507336.1:p.Phe256Ser | |
| ENST00000682231.1:n.178T>C | ||
| ENST00000682438.1:n.3159T>C | ||
| ENST00000682499.1:n.1981T>C | ||
| ENST00000682541.1:c.*58T>C | ENSP00000507673.1:n.*58T>C | |
| ENST00000682640.1:n.864T>C | ||
| ENST00000682667.1:n.1325T>C | ||
| ENST00000682687.1:c.*112T>C | ENSP00000507945.1:n.*112T>C | |
| ENST00000682727.1:c.1151T>C | ENSP00000507393.1:p.Phe384Ser | |
| ENST00000682876.1:c.1289T>C | ENSP00000508389.1:p.Phe430Ser | |
| ENST00000683098.1:c.814T>C | ENSP00000507670.1:p.Leu272= | |
| ENST00000683258.1:c.*881T>C | ENSP00000507448.1:n.*881T>C | |
| ENST00000683339.1:c.944T>C | ENSP00000507758.1:p.Phe315Ser | |
| ENST00000683403.1:c.1070T>C | ENSP00000507896.1:p.Phe357Ser | |
| ENST00000683429.1:c.767T>C | ENSP00000507697.1:p.Phe256Ser | |
| ENST00000683789.1:c.1046T>C | ENSP00000507012.1:p.Phe349Ser | |
| ENST00000683847.1:n.1330T>C | ||
| ENST00000683882.1:c.*101T>C | ENSP00000506735.1:n.*101T>C | |
| ENST00000684024.1:c.*831T>C | ENSP00000507175.1:n.*831T>C | |
| ENST00000684132.1:c.88T>C | ||
| ENST00000684254.1:c.*886T>C | ENSP00000508001.1:n.*886T>C | |
| ENST00000684310.1:c.326T>C | ENSP00000507550.1:p.Phe109Ser | |
| ENST00000684474.1:n.796T>C | ||
| ENST00000684530.1:c.335-2876T>C | ENSP00000507439.1:n.335-2876T>C | |
| ENST00000684686.1:n.779T>C | ||
| ENST00000340941.11:c.1160T>C MANE Select | ENSP00000343657.6:p.Phe387Ser | |
| ENST00000340941.10:c.1160T>C | ENSP00000343657.6:p.Phe387Ser | |
| ENST00000509539.2:c.476T>C | ENSP00000425474.2:p.Phe159Ser | |
| ENST00000512218.6:c.*112T>C | ENSP00000423202.2:n.*112T>C | |
| NM_022132.4:c.1160T>C | NP_071415.1:p.Phe387Ser | |
| XM_005248567.1:c.1046T>C | XP_005248624.1:p.Phe349Ser | |
| NM_001363147.1:c.1046T>C | NP_001350076.1:p.Phe349Ser | |
| XR_001742172.1:n.1248T>C | ||
| NM_022132.5:c.1160T>C MANE Select | NP_071415.1:p.Phe387Ser |