Revel Score:
ENST00000382292 (MANE Select)
0.348
ENST00000402364
0.348
ENST00000382298
0.348
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.23333954G>A , CM000675.2:g.23333954G>A | GRCh38 |
| NC_000013.10:g.23908093G>A , CM000675.1:g.23908093G>A | GRCh37 |
| NC_000013.9:g.22806093G>A | NCBI36 |
| NG_012342.1:g.104749C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682775.1:c.2185+19831C>T | ENSP00000508399.1:n.2185+19831C>T | |
| ENST00000682944.1:c.9949C>T | ENSP00000507173.1:p.His3317Tyr | |
| ENST00000683210.1:c.2185+19831C>T | ENSP00000506739.1:n.2185+19831C>T | |
| ENST00000683270.1:c.6445+3468C>T | ENSP00000507624.1:n.6445+3468C>T | |
| ENST00000683367.1:c.2177-4470C>T | ENSP00000507780.1:n.2177-4470C>T | |
| ENST00000683489.1:c.2292-4002C>T | ENSP00000508403.1:n.2292-4002C>T | |
| ENST00000683680.1:c.2319-4002C>T | ENSP00000507223.1:n.2319-4002C>T | |
| ENST00000684163.1:c.2204-4470C>T | ENSP00000508262.1:n.2204-4470C>T | |
| ENST00000684196.1:n.4543-4470C>T | ||
| ENST00000684325.1:c.2186-12280C>T | ENSP00000508121.1:n.2186-12280C>T | |
| ENST00000684385.1:c.2221-4470C>T | ENSP00000507855.1:n.2221-4470C>T | |
| ENST00000684497.1:c.2186-11310C>T | ENSP00000507057.1:n.2186-11310C>T | |
| ENST00000382292.9:c.9922C>T MANE Select | ENSP00000371729.3:p.His3308Tyr | |
| ENST00000423156.2:c.2186-4470C>T | ENSP00000390925.2:n.2186-4470C>T | |
| ENST00000455470.6:c.2432-4470C>T | ENSP00000406565.2:n.2432-4470C>T | |
| ENST00000382292.7:c.9922C>T | ENSP00000371729.3:p.His3308Tyr | |
| ENST00000382298.7:c.9922C>T | ENSP00000371735.3:p.His3308Tyr | |
| ENST00000402364.1:c.7672C>T | ENSP00000385844.1:p.His2558Tyr | |
| ENST00000423156.1:c.1058-4470C>T | ENSP00000390925.1:n.1058-4470C>T | |
| ENST00000455470.5:c.2130-4470C>T | ||
| NM_001278055.1:c.9481C>T | NP_001264984.1:p.His3161Tyr | |
| NM_014363.5:c.9922C>T | NP_055178.3:p.His3308Tyr | |
| XM_005266338.1:c.9949C>T | XP_005266395.1:p.His3317Tyr | |
| XM_011535038.1:c.9973C>T | XP_011533340.1:p.His3325Tyr | |
| XM_011535039.1:c.9940C>T | XP_011533341.1:p.His3314Tyr | |
| XM_005266338.2:c.9949C>T | XP_005266395.1:p.His3317Tyr | |
| XM_011535039.2:c.9940C>T | XP_011533341.1:p.His3314Tyr | |
| XM_017020539.1:c.9913C>T | XP_016876028.1:p.His3305Tyr | |
| XM_024449337.1:c.9949C>T | XP_024305105.1:p.His3317Tyr | |
| NM_014363.6:c.9922C>T MANE Select | NP_055178.3:p.His3308Tyr | |
| NM_001278055.2:c.9481C>T | NP_001264984.1:p.His3161Tyr |