Revel Score:
ENST00000487664
0.412
ENST00000298480
0.412
ENST00000371757 (MANE Select)
0.412
ENST00000486577
0.412
ENST00000491806
0.412
ENST00000488444
0.412
ENST00000490355
0.412
ENST00000263604
0.412
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.135765732C>T , CM000671.2:g.135765732C>T | GRCh38 |
| NC_000009.11:g.138657578C>T , CM000671.1:g.138657578C>T | GRCh37 |
| NC_000009.10:g.137797399C>T | NCBI36 |
| NG_033070.1:g.68548C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371757.7:c.1309C>T MANE Select | ENSP00000360822.2:p.Leu437Phe | |
| ENST00000636995.1:n.36C>T | ||
| ENST00000637798.1:n.48C>T | ||
| ENST00000674572.1:c.1150C>T | ENSP00000501742.1:p.Leu384Phe | |
| ENST00000675090.1:c.1057C>T | ENSP00000501833.1:p.Leu353Phe | |
| ENST00000675399.1:c.1057C>T | ENSP00000501932.1:p.Leu353Phe | |
| ENST00000676421.1:c.1066C>T | ENSP00000502322.1:p.Leu356Phe | |
| ENST00000263604.5:c.1210C>T | ENSP00000263604.4:p.Leu404Phe | |
| ENST00000371757.6:c.1309C>T | ENSP00000360822.2:p.Leu437Phe | |
| ENST00000460750.5:c.*919C>T | ENSP00000418777.1:n.*919C>T | |
| ENST00000486577.6:c.1192C>T | ENSP00000417578.3:p.Leu398Phe | |
| ENST00000487664.5:c.1309C>T | ENSP00000417851.2:p.Leu437Phe | |
| ENST00000488444.6:c.1252C>T | ENSP00000419007.3:p.Leu418Phe | |
| ENST00000490355.6:c.1252C>T | ENSP00000418003.3:p.Leu418Phe | |
| ENST00000490363.3:n.1128C>T | ||
| ENST00000491806.6:c.1252C>T | ENSP00000419086.3:p.Leu418Phe | |
| ENST00000628528.2:c.1174C>T | ENSP00000486374.1:p.Leu392Phe | |
| ENST00000630792.2:c.1150C>T | ENSP00000486486.1:p.Leu384Phe | |
| ENST00000631073.2:c.1252C>T | ENSP00000486130.1:p.Leu418Phe | |
| NM_001272003.1:c.1174C>T | NP_001258932.1:p.Leu392Phe | |
| NM_020822.2:c.1309C>T | NP_065873.2:p.Leu437Phe | |
| XM_011518877.1:c.1444C>T | XP_011517179.1:p.Leu482Phe | |
| XM_011518878.1:c.1453C>T | XP_011517180.1:p.Leu485Phe | |
| XM_011518879.1:c.1444C>T | XP_011517181.1:p.Leu482Phe | |
| XM_011518880.1:c.1210C>T | XP_011517182.1:p.Leu404Phe | |
| XM_011518881.1:c.799C>T | XP_011517183.1:p.Leu267Phe | |
| XM_011518877.3:c.1444C>T | XP_011517179.1:p.Leu482Phe | |
| XM_011518878.3:c.1453C>T | XP_011517180.1:p.Leu485Phe | |
| XM_011518879.3:c.1444C>T | XP_011517181.1:p.Leu482Phe | |
| XM_011518881.3:c.799C>T | XP_011517183.1:p.Leu267Phe | |
| XM_017014931.1:c.1243C>T | XP_016870420.1:p.Leu415Phe | |
| XM_017014932.1:c.1066C>T | XP_016870421.1:p.Leu356Phe | |
| XM_017014933.1:c.799C>T | XP_016870422.1:p.Leu267Phe | |
| XM_024447617.1:c.799C>T | XP_024303385.1:p.Leu267Phe | |
| XM_024447618.1:c.799C>T | XP_024303386.1:p.Leu267Phe | |
| NM_020822.3:c.1309C>T MANE Select | NP_065873.2:p.Leu437Phe | |
| NM_001272003.2:c.1174C>T | NP_001258932.1:p.Leu392Phe |