Revel Score:
ENST00000357555
0.810
ENST00000369062
0.810
ENST00000369061
0.810
ENST00000358487 (MANE Select)
0.810
ENST00000356226
0.810
ENST00000369060
0.810
ENST00000369059
0.810
ENST00000429361
0.810
ENST00000346997
0.810
ENST00000457416 (MANE Plus Clinical)
0.810
ENST00000351936
0.810
ENST00000360144
0.810
ENST00000369056
0.810
ENST00000369058
0.810
ENST00000336553
0.810
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.121488005T>G , CM000672.2:g.121488005T>G | GRCh38 |
| NC_000010.10:g.123247519T>G , CM000672.1:g.123247519T>G | GRCh37 |
| NC_000010.9:g.123237509T>G | NCBI36 |
| NG_012449.1:g.115454A>C | |
| NG_012449.2:g.115454A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000457416.7:c.1975A>C MANE Plus Clinical | ENSP00000410294.2:p.Lys659Gln | |
| ENST00000351936.11:c.1966A>C | ENSP00000309878.10:p.Lys656Gln | |
| ENST00000638709.2:c.796A>C | ENSP00000491912.2:p.Lys266Gln | |
| ENST00000682296.1:n.1314A>C | ||
| ENST00000682550.1:c.1621A>C | ENSP00000507633.1:p.Lys541Gln | |
| ENST00000682772.1:c.796A>C | ENSP00000506848.1:p.Lys266Gln | |
| ENST00000682904.1:n.792A>C | ||
| ENST00000683029.1:n.384A>C | ||
| ENST00000683211.1:c.1966A>C | ENSP00000508257.1:p.Lys656Gln | |
| ENST00000683250.1:c.*674A>C | ENSP00000506847.1:n.*674A>C | |
| ENST00000683418.1:n.4313A>C | ||
| ENST00000684153.1:c.1621A>C | ENSP00000506937.1:p.Lys541Gln | |
| ENST00000684516.1:n.2985A>C | ||
| ENST00000358487.10:c.1972A>C MANE Select | ENSP00000351276.6:p.Lys658Gln | |
| ENST00000336553.10:c.1699A>C | ENSP00000337665.6:p.Lys567Gln | |
| ENST00000346997.6:c.1966A>C | ENSP00000263451.5:p.Lys656Gln | |
| ENST00000351936.10:c.1972A>C | ENSP00000309878.9:p.Lys658Gln | |
| ENST00000356226.8:c.1621A>C | ENSP00000348559.4:p.Lys541Gln | |
| ENST00000357555.9:c.1705A>C | ENSP00000350166.5:p.Lys569Gln | |
| ENST00000358487.9:c.1972A>C | ENSP00000351276.5:p.Lys658Gln | |
| ENST00000360144.7:c.1708A>C | ENSP00000353262.3:p.Lys570Gln | |
| ENST00000369056.5:c.1975A>C | ENSP00000358052.1:p.Lys659Gln | |
| ENST00000369058.7:c.1975A>C | ENSP00000358054.3:p.Lys659Gln | |
| ENST00000369059.5:c.1630A>C | ENSP00000358055.1:p.Lys544Gln | |
| ENST00000369060.8:c.1624A>C | ENSP00000358056.4:p.Lys542Gln | |
| ENST00000369061.8:c.1636A>C | ENSP00000358057.4:p.Lys546Gln | |
| ENST00000429361.5:c.748A>C | ENSP00000404219.1:p.Lys250Gln | |
| ENST00000457416.6:c.1975A>C | ENSP00000410294.2:p.Lys659Gln | |
| ENST00000478859.5:c.1288A>C | ENSP00000474011.1:p.Lys430Gln | |
| ENST00000604236.5:c.*1019A>C | ENSP00000474109.1:n.*1019A>C | |
| ENST00000613048.4:c.1705A>C | ENSP00000484154.1:p.Lys569Gln | |
| NM_000141.4:c.1972A>C | NP_000132.3:p.Lys658Gln | |
| NM_001144913.1:c.1975A>C | NP_001138385.1:p.Lys659Gln | |
| NM_001144914.1:c.1636A>C | NP_001138386.1:p.Lys546Gln | |
| NM_001144915.1:c.1705A>C | NP_001138387.1:p.Lys569Gln | |
| NM_001144916.1:c.1627A>C | NP_001138388.1:p.Lys543Gln | |
| NM_001144917.1:c.1624A>C | NP_001138389.1:p.Lys542Gln | |
| NM_001144918.1:c.1621A>C | NP_001138390.1:p.Lys541Gln | |
| NM_001144919.1:c.1708A>C | NP_001138391.1:p.Lys570Gln | |
| NM_022970.3:c.1975A>C | NP_075259.4:p.Lys659Gln | |
| NM_023029.2:c.1705A>C | NP_075418.1:p.Lys569Gln | |
| NR_073009.1:n.2422A>C | ||
| XM_006717708.2:c.2026A>C | XP_006717771.1:p.Lys676Gln | |
| XM_006717709.2:c.2023A>C | XP_006717772.1:p.Lys675Gln | |
| XM_006717710.2:c.2032A>C | XP_006717773.1:p.Lys678Gln | |
| XM_006717711.2:c.1765A>C | XP_006717774.1:p.Lys589Gln | |
| XM_006717712.2:c.1687A>C | XP_006717775.1:p.Lys563Gln | |
| XM_006717713.2:c.2029A>C | XP_006717776.1:p.Lys677Gln | |
| XM_011539510.1:c.1288A>C | XP_011537812.1:p.Lys430Gln | |
| NM_001320654.1:c.1288A>C | NP_001307583.1:p.Lys430Gln | |
| NM_001320658.1:c.1966A>C | NP_001307587.1:p.Lys656Gln | |
| XM_006717708.3:c.2026A>C | XP_006717771.1:p.Lys676Gln | |
| XM_006717710.4:c.2032A>C | XP_006717773.1:p.Lys678Gln | |
| XM_017015920.2:c.2026A>C | XP_016871409.1:p.Lys676Gln | |
| XM_017015921.2:c.2023A>C | XP_016871410.1:p.Lys675Gln | |
| XM_017015924.2:c.1684A>C | XP_016871413.1:p.Lys562Gln | |
| XM_017015925.2:c.1678A>C | XP_016871414.1:p.Lys560Gln | |
| XM_024447887.1:c.1762A>C | XP_024303655.1:p.Lys588Gln | |
| XM_024447888.1:c.1759A>C | XP_024303656.1:p.Lys587Gln | |
| XM_024447889.1:c.1756A>C | XP_024303657.1:p.Lys586Gln | |
| XM_024447890.1:c.1765A>C | XP_024303658.1:p.Lys589Gln | |
| XM_024447891.1:c.1687A>C | XP_024303659.1:p.Lys563Gln | |
| XM_024447892.1:c.802A>C | XP_024303660.1:p.Lys268Gln | |
| NM_000141.5:c.1972A>C MANE Select | NP_000132.3:p.Lys658Gln | |
| NM_001144917.2:c.1624A>C | NP_001138389.1:p.Lys542Gln | |
| NM_001144918.2:c.1621A>C | NP_001138390.1:p.Lys541Gln | |
| NM_001144919.2:c.1708A>C | NP_001138391.1:p.Lys570Gln | |
| NM_001320658.2:c.1966A>C | NP_001307587.1:p.Lys656Gln | |
| NR_073009.2:n.2408A>C | ||
| NM_001144915.2:c.1705A>C | NP_001138387.1:p.Lys569Gln | |
| NM_001144916.2:c.1627A>C | NP_001138388.1:p.Lys543Gln | |
| NM_001320654.2:c.1288A>C | NP_001307583.1:p.Lys430Gln |