Revel Score:
ENST00000260947 (MANE Select)
0.053
ENST00000432456
0.053
ENST00000449967
0.058
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.214728956T>C , CM000664.2:g.214728956T>C | GRCh38 |
| NC_000002.11:g.215593680T>C , CM000664.1:g.215593680T>C | GRCh37 |
| NC_000002.10:g.215301925T>C | NCBI36 |
| NG_012047.2:g.85749A>G | |
| NG_012047.3:g.85756A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260947.9:c.2054A>G MANE Select | ENSP00000260947.4:p.His685Arg | |
| ENST00000421162.2:c.701A>G | ENSP00000392245.2:p.His234Arg | |
| ENST00000613192.2:c.*117A>G | ENSP00000483275.2:n.*117A>G | |
| ENST00000613374.5:c.644A>G | ENSP00000484464.1:p.His215Arg | |
| ENST00000613706.5:c.1646A>G | ENSP00000484976.2:p.His549Arg | |
| ENST00000617164.5:c.1997A>G | ENSP00000480470.1:p.His666Arg | |
| ENST00000619009.5:c.515A>G | ENSP00000482293.1:p.His172Arg | |
| ENST00000650978.1:c.3429A>G | ||
| ENST00000260947.8:c.2054A>G | ENSP00000260947.4:p.His685Arg | |
| ENST00000432456.5:c.197A>G | ||
| ENST00000455743.5:c.*1674A>G | ENSP00000412186.1:n.*1674A>G | |
| ENST00000471590.5:n.389A>G | ||
| ENST00000613192.1:c.224A>G | ENSP00000483275.1:p.His75Arg | |
| ENST00000613374.4:c.644A>G | ENSP00000484464.1:p.His215Arg | |
| ENST00000613706.4:c.701A>G | ENSP00000484976.1:p.His234Arg | |
| ENST00000617164.4:c.1997A>G | ENSP00000480470.1:p.His666Arg | |
| ENST00000619009.4:c.515A>G | ENSP00000482293.1:p.His172Arg | |
| ENST00000620057.4:c.*720A>G | ENSP00000481988.1:n.*720A>G | |
| NM_000465.3:c.2054A>G | NP_000456.2:p.His685Arg | |
| NM_001282543.1:c.1997A>G | NP_001269472.1:p.His666Arg | |
| NM_001282545.1:c.701A>G | NP_001269474.1:p.His234Arg | |
| NM_001282548.1:c.644A>G | NP_001269477.1:p.His215Arg | |
| NM_001282549.1:c.515A>G | NP_001269478.1:p.His172Arg | |
| NR_104212.1:n.2047A>G | ||
| NR_104215.1:n.1990A>G | ||
| NR_104216.1:n.1246A>G | ||
| XM_011511567.1:c.2000A>G | XP_011509869.1:p.His667Arg | |
| XM_017004613.1:c.2153A>G | XP_016860102.1:p.His718Arg | |
| XR_002959322.1:n.2420A>G | ||
| NM_000465.4:c.2054A>G MANE Select | NP_000456.2:p.His685Arg | |
| NM_001282543.2:c.1997A>G | NP_001269472.1:p.His666Arg | |
| NM_001282545.2:c.701A>G | NP_001269474.1:p.His234Arg | |
| NM_001282548.2:c.644A>G | NP_001269477.1:p.His215Arg | |
| NM_001282549.2:c.515A>G | NP_001269478.1:p.His172Arg | |
| NR_104212.2:n.2019A>G | ||
| NR_104215.2:n.1962A>G | ||
| NR_104216.2:n.1218A>G |