Revel Score:
ENST00000487664
0.427
ENST00000298480
0.427
ENST00000371757 (MANE Select)
0.427
ENST00000473941
0.427
ENST00000486577
0.427
ENST00000491806
0.427
ENST00000488444
0.427
ENST00000490355
0.427
ENST00000263604
0.427
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.135758495C>T , CM000671.2:g.135758495C>T | GRCh38 |
| NC_000009.11:g.138650341C>T , CM000671.1:g.138650341C>T | GRCh37 |
| NC_000009.10:g.137790162C>T | NCBI36 |
| NG_033070.1:g.61311C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371757.7:c.841C>T MANE Select | ENSP00000360822.2:p.Leu281Phe | |
| ENST00000674572.1:c.682C>T | ENSP00000501742.1:p.Leu228Phe | |
| ENST00000675090.1:c.589C>T | ENSP00000501833.1:p.Leu197Phe | |
| ENST00000675399.1:c.589C>T | ENSP00000501932.1:p.Leu197Phe | |
| ENST00000676421.1:c.589C>T | ENSP00000502322.1:p.Leu197Phe | |
| ENST00000263604.5:c.742C>T | ENSP00000263604.4:p.Leu248Phe | |
| ENST00000371757.6:c.841C>T | ENSP00000360822.2:p.Leu281Phe | |
| ENST00000460750.5:c.*451C>T | ENSP00000418777.1:n.*451C>T | |
| ENST00000473941.5:c.682C>T | ENSP00000420764.1:p.Leu228Phe | |
| ENST00000486577.6:c.724C>T | ENSP00000417578.3:p.Leu242Phe | |
| ENST00000487664.5:c.841C>T | ENSP00000417851.2:p.Leu281Phe | |
| ENST00000488444.6:c.784C>T | ENSP00000419007.3:p.Leu262Phe | |
| ENST00000490355.6:c.784C>T | ENSP00000418003.3:p.Leu262Phe | |
| ENST00000490363.3:n.660C>T | ||
| ENST00000491806.6:c.784C>T | ENSP00000419086.3:p.Leu262Phe | |
| ENST00000628528.2:c.697C>T | ENSP00000486374.1:p.Leu233Phe | |
| ENST00000630792.2:c.682C>T | ENSP00000486486.1:p.Leu228Phe | |
| ENST00000631073.2:c.784C>T | ENSP00000486130.1:p.Leu262Phe | |
| NM_001272003.1:c.697C>T | NP_001258932.1:p.Leu233Phe | |
| NM_020822.2:c.841C>T | NP_065873.2:p.Leu281Phe | |
| XM_011518877.1:c.976C>T | XP_011517179.1:p.Leu326Phe | |
| XM_011518878.1:c.976C>T | XP_011517180.1:p.Leu326Phe | |
| XM_011518879.1:c.976C>T | XP_011517181.1:p.Leu326Phe | |
| XM_011518880.1:c.742C>T | XP_011517182.1:p.Leu248Phe | |
| XM_011518881.1:c.322C>T | XP_011517183.1:p.Leu108Phe | |
| XM_011518877.3:c.976C>T | XP_011517179.1:p.Leu326Phe | |
| XM_011518878.3:c.976C>T | XP_011517180.1:p.Leu326Phe | |
| XM_011518879.3:c.976C>T | XP_011517181.1:p.Leu326Phe | |
| XM_011518881.3:c.322C>T | XP_011517183.1:p.Leu108Phe | |
| XM_017014931.1:c.766C>T | XP_016870420.1:p.Leu256Phe | |
| XM_017014932.1:c.589C>T | XP_016870421.1:p.Leu197Phe | |
| XM_017014933.1:c.322C>T | XP_016870422.1:p.Leu108Phe | |
| XM_024447617.1:c.322C>T | XP_024303385.1:p.Leu108Phe | |
| XM_024447618.1:c.322C>T | XP_024303386.1:p.Leu108Phe | |
| NM_020822.3:c.841C>T MANE Select | NP_065873.2:p.Leu281Phe | |
| NM_001272003.2:c.697C>T | NP_001258932.1:p.Leu233Phe |