Revel Score:
ENST00000418337
0.902
ENST00000287878 (MANE Select)
0.902
ENST00000492843
0.902
ENST00000433631
0.902
ENST00000392801
0.902
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.151560613T>C , CM000669.2:g.151560613T>C | GRCh38 |
| NC_000007.13:g.151257699T>C , CM000669.1:g.151257699T>C | GRCh37 |
| NC_000007.12:g.150888632T>C | NCBI36 |
| NG_007486.1:g.321618A>G | |
| NG_007486.2:g.321619A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000478989.7:c.*325A>G | ENSP00000420645.3:n.*325A>G | |
| ENST00000652321.2:c.1586A>G | ENSP00000498886.2:p.His529Arg | |
| ENST00000287878.9:c.1589A>G MANE Select | ENSP00000287878.3:p.His530Arg | |
| ENST00000476632.2:c.866A>G | ENSP00000419493.2:p.His289Arg | |
| ENST00000492843.6:c.1214A>G | ENSP00000419577.2:p.His405Arg | |
| ENST00000650664.1:n.1304A>G | ||
| ENST00000650851.1:n.1083A>G | ||
| ENST00000650858.1:c.806A>G | ENSP00000498384.1:p.His269Arg | |
| ENST00000650948.1:n.3975A>G | ||
| ENST00000651188.1:c.*702A>G | ENSP00000498557.1:n.*702A>G | |
| ENST00000651303.1:c.*908A>G | ENSP00000498428.1:n.*908A>G | |
| ENST00000651378.1:c.866A>G | ENSP00000499103.1:p.His289Arg | |
| ENST00000651764.1:c.1457A>G | ENSP00000498796.1:p.His486Arg | |
| ENST00000651836.1:c.1779A>G | ENSP00000499156.1:n.1779A>G | |
| ENST00000651954.1:n.1805A>G | ||
| ENST00000652047.1:c.1454A>G | ENSP00000499111.1:p.His485Arg | |
| ENST00000652136.1:n.2136A>G | ||
| ENST00000652159.1:c.1457A>G | ENSP00000499025.1:p.His486Arg | |
| ENST00000652397.1:c.*325A>G | ENSP00000498351.1:n.*325A>G | |
| ENST00000287878.8:c.1589A>G | ENSP00000287878.3:p.His530Arg | |
| ENST00000392801.6:c.1457A>G | ENSP00000376549.2:p.His486Arg | |
| ENST00000418337.6:c.866A>G | ENSP00000387386.2:p.His289Arg | |
| ENST00000479461.1:n.241A>G | ||
| ENST00000485183.1:n.242A>G | ||
| ENST00000492843.5:c.1217A>G | ENSP00000419577.1:p.His406Arg | |
| NM_001040633.1:c.1457A>G | NP_001035723.1:p.His486Arg | |
| NM_001304527.1:c.1214A>G | NP_001291456.1:p.His405Arg | |
| NM_001304531.1:c.866A>G | NP_001291460.1:p.His289Arg | |
| NM_016203.3:c.1589A>G | NP_057287.2:p.His530Arg | |
| NM_024429.1:c.866A>G | NP_077747.1:p.His289Arg | |
| XM_005250002.2:c.1589A>G | XP_005250059.1:p.His530Arg | |
| XM_005250004.2:c.1457A>G | XP_005250061.1:p.His486Arg | |
| XM_005250006.3:c.1217A>G | XP_005250063.1:p.His406Arg | |
| XM_006716021.2:c.1577A>G | XP_006716084.1:p.His526Arg | |
| XM_011516282.1:c.1574A>G | XP_011514584.1:p.His525Arg | |
| XM_011516283.1:c.1577A>G | XP_011514585.1:p.His526Arg | |
| XM_011516284.1:c.1574A>G | XP_011514586.1:p.His525Arg | |
| XM_011516285.1:c.866A>G | XP_011514587.1:p.His289Arg | |
| XM_011516286.1:c.842A>G | XP_011514588.1:p.His281Arg | |
| XM_011516287.1:c.806A>G | XP_011514589.1:p.His269Arg | |
| NM_001363698.1:c.1217A>G | NP_001350627.1:p.His406Arg | |
| XM_005250002.4:c.1589A>G | XP_005250059.1:p.His530Arg | |
| XM_005250004.4:c.1457A>G | XP_005250061.1:p.His486Arg | |
| XM_005250006.5:c.1217A>G | XP_005250063.1:p.His406Arg | |
| XM_011516285.2:c.866A>G | XP_011514587.1:p.His289Arg | |
| XM_011516286.2:c.842A>G | XP_011514588.1:p.His281Arg | |
| XM_017012268.2:c.1454A>G | XP_016867757.1:p.His485Arg | |
| XM_017012269.1:c.1586A>G | XP_016867758.1:p.His529Arg | |
| XM_017012270.1:c.1457A>G | XP_016867759.1:p.His486Arg | |
| XM_017012271.2:c.1454A>G | XP_016867760.1:p.His485Arg | |
| XM_017012272.1:c.1454A>G | XP_016867761.1:p.His485Arg | |
| XM_017012274.2:c.863A>G | XP_016867763.1:p.His288Arg | |
| XM_017012275.2:c.806A>G | XP_016867764.1:p.His269Arg | |
| XM_017012276.2:c.863A>G | XP_016867765.1:p.His288Arg | |
| XM_017012277.2:c.842A>G | XP_016867766.1:p.His281Arg | |
| XM_017012278.1:c.806A>G | XP_016867767.1:p.His269Arg | |
| XM_017012279.2:c.806A>G | XP_016867768.1:p.His269Arg | |
| XM_017012280.2:c.806A>G | XP_016867769.1:p.His269Arg | |
| XM_017012281.2:c.806A>G | XP_016867770.1:p.His269Arg | |
| XM_024446786.1:c.1457A>G | XP_024302554.1:p.His486Arg | |
| XM_024446787.1:c.866A>G | XP_024302555.1:p.His289Arg | |
| XM_024446788.1:c.863A>G | XP_024302556.1:p.His288Arg | |
| XM_024446789.1:c.866A>G | XP_024302557.1:p.His289Arg | |
| NM_016203.4:c.1589A>G MANE Select | NP_057287.2:p.His530Arg | |
| NM_001040633.2:c.1457A>G | NP_001035723.1:p.His486Arg | |
| NM_001304527.2:c.1214A>G | NP_001291456.1:p.His405Arg | |
| NM_001304531.2:c.866A>G | NP_001291460.1:p.His289Arg | |
| NM_001363698.2:c.1217A>G | NP_001350627.1:p.His406Arg | |
| NM_024429.2:c.866A>G | NP_077747.1:p.His289Arg |