Revel Score:
ENST00000357555
0.753
ENST00000369062
0.753
ENST00000369061
0.753
ENST00000358487 (MANE Select)
0.753
ENST00000356226
0.753
ENST00000369060
0.753
ENST00000369059
0.753
ENST00000429361
0.753
ENST00000346997
0.753
ENST00000457416 (MANE Plus Clinical)
0.753
ENST00000351936
0.753
ENST00000360144
0.753
ENST00000369056
0.753
ENST00000369058
0.753
ENST00000336553
0.753
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.121498597T>C , CM000672.2:g.121498597T>C | GRCh38 |
| NC_000010.10:g.123258111T>C , CM000672.1:g.123258111T>C | GRCh37 |
| NC_000010.9:g.123248101T>C | NCBI36 |
| NG_012449.1:g.104862A>G | |
| NG_012449.2:g.104862A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000457416.7:c.1573A>G MANE Plus Clinical | ENSP00000410294.2:p.Thr525Ala | |
| ENST00000351936.11:c.1564A>G | ENSP00000309878.10:p.Thr522Ala | |
| ENST00000638709.2:c.394A>G | ENSP00000491912.2:p.Thr132Ala | |
| ENST00000682296.1:n.912A>G | ||
| ENST00000682550.1:c.1219A>G | ENSP00000507633.1:p.Thr407Ala | |
| ENST00000682772.1:c.394A>G | ENSP00000506848.1:p.Thr132Ala | |
| ENST00000682904.1:n.390A>G | ||
| ENST00000683211.1:c.1564A>G | ENSP00000508257.1:p.Thr522Ala | |
| ENST00000683250.1:c.*272A>G | ENSP00000506847.1:n.*272A>G | |
| ENST00000683418.1:n.3911A>G | ||
| ENST00000684153.1:c.1219A>G | ENSP00000506937.1:p.Thr407Ala | |
| ENST00000684516.1:n.2583A>G | ||
| ENST00000358487.10:c.1570A>G MANE Select | ENSP00000351276.6:p.Thr524Ala | |
| ENST00000336553.10:c.1297A>G | ENSP00000337665.6:p.Thr433Ala | |
| ENST00000346997.6:c.1564A>G | ENSP00000263451.5:p.Thr522Ala | |
| ENST00000351936.10:c.1570A>G | ENSP00000309878.9:p.Thr524Ala | |
| ENST00000356226.8:c.1219A>G | ENSP00000348559.4:p.Thr407Ala | |
| ENST00000357555.9:c.1303A>G | ENSP00000350166.5:p.Thr435Ala | |
| ENST00000358487.9:c.1570A>G | ENSP00000351276.5:p.Thr524Ala | |
| ENST00000360144.7:c.1306A>G | ENSP00000353262.3:p.Thr436Ala | |
| ENST00000369056.5:c.1573A>G | ENSP00000358052.1:p.Thr525Ala | |
| ENST00000369058.7:c.1573A>G | ENSP00000358054.3:p.Thr525Ala | |
| ENST00000369059.5:c.1228A>G | ENSP00000358055.1:p.Thr410Ala | |
| ENST00000369060.8:c.1222A>G | ENSP00000358056.4:p.Thr408Ala | |
| ENST00000369061.8:c.1234A>G | ENSP00000358057.4:p.Thr412Ala | |
| ENST00000429361.5:c.346A>G | ENSP00000404219.1:p.Thr116Ala | |
| ENST00000457416.6:c.1573A>G | ENSP00000410294.2:p.Thr525Ala | |
| ENST00000478859.5:c.886A>G | ENSP00000474011.1:p.Thr296Ala | |
| ENST00000604236.5:c.*617A>G | ENSP00000474109.1:n.*617A>G | |
| ENST00000613048.4:c.1303A>G | ENSP00000484154.1:p.Thr435Ala | |
| NM_000141.4:c.1570A>G | NP_000132.3:p.Thr524Ala | |
| NM_001144913.1:c.1573A>G | NP_001138385.1:p.Thr525Ala | |
| NM_001144914.1:c.1234A>G | NP_001138386.1:p.Thr412Ala | |
| NM_001144915.1:c.1303A>G | NP_001138387.1:p.Thr435Ala | |
| NM_001144916.1:c.1225A>G | NP_001138388.1:p.Thr409Ala | |
| NM_001144917.1:c.1222A>G | NP_001138389.1:p.Thr408Ala | |
| NM_001144918.1:c.1219A>G | NP_001138390.1:p.Thr407Ala | |
| NM_001144919.1:c.1306A>G | NP_001138391.1:p.Thr436Ala | |
| NM_022970.3:c.1573A>G | NP_075259.4:p.Thr525Ala | |
| NM_023029.2:c.1303A>G | NP_075418.1:p.Thr435Ala | |
| NR_073009.1:n.2020A>G | ||
| XM_006717708.2:c.1624A>G | XP_006717771.1:p.Thr542Ala | |
| XM_006717709.2:c.1621A>G | XP_006717772.1:p.Thr541Ala | |
| XM_006717710.2:c.1630A>G | XP_006717773.1:p.Thr544Ala | |
| XM_006717711.2:c.1363A>G | XP_006717774.1:p.Thr455Ala | |
| XM_006717712.2:c.1285A>G | XP_006717775.1:p.Thr429Ala | |
| XM_006717713.2:c.1627A>G | XP_006717776.1:p.Thr543Ala | |
| XM_011539510.1:c.886A>G | XP_011537812.1:p.Thr296Ala | |
| NM_001320654.1:c.886A>G | NP_001307583.1:p.Thr296Ala | |
| NM_001320658.1:c.1564A>G | NP_001307587.1:p.Thr522Ala | |
| XM_006717708.3:c.1624A>G | XP_006717771.1:p.Thr542Ala | |
| XM_006717710.4:c.1630A>G | XP_006717773.1:p.Thr544Ala | |
| XM_017015920.2:c.1624A>G | XP_016871409.1:p.Thr542Ala | |
| XM_017015921.2:c.1621A>G | XP_016871410.1:p.Thr541Ala | |
| XM_017015924.2:c.1282A>G | XP_016871413.1:p.Thr428Ala | |
| XM_017015925.2:c.1276A>G | XP_016871414.1:p.Thr426Ala | |
| XM_024447887.1:c.1360A>G | XP_024303655.1:p.Thr454Ala | |
| XM_024447888.1:c.1357A>G | XP_024303656.1:p.Thr453Ala | |
| XM_024447889.1:c.1354A>G | XP_024303657.1:p.Thr452Ala | |
| XM_024447890.1:c.1363A>G | XP_024303658.1:p.Thr455Ala | |
| XM_024447891.1:c.1285A>G | XP_024303659.1:p.Thr429Ala | |
| XM_024447892.1:c.400A>G | XP_024303660.1:p.Thr134Ala | |
| NM_000141.5:c.1570A>G MANE Select | NP_000132.3:p.Thr524Ala | |
| NM_001144917.2:c.1222A>G | NP_001138389.1:p.Thr408Ala | |
| NM_001144918.2:c.1219A>G | NP_001138390.1:p.Thr407Ala | |
| NM_001144919.2:c.1306A>G | NP_001138391.1:p.Thr436Ala | |
| NM_001320658.2:c.1564A>G | NP_001307587.1:p.Thr522Ala | |
| NR_073009.2:n.2006A>G | ||
| NM_001144915.2:c.1303A>G | NP_001138387.1:p.Thr435Ala | |
| NM_001144916.2:c.1225A>G | NP_001138388.1:p.Thr409Ala | |
| NM_001320654.2:c.886A>G | NP_001307583.1:p.Thr296Ala |