Revel Score:
ENST00000457016
0.834
ENST00000507379
0.834
ENST00000257430 (MANE Select)
0.834
ENST00000508376
0.834
ENST00000512211
0.834
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112835165G>C , CM000667.2:g.112835165G>C | GRCh38 |
| NC_000005.9:g.112170862G>C , CM000667.1:g.112170862G>C | GRCh37 |
| NC_000005.8:g.112198761G>C | NCBI36 |
| NG_008481.4:g.147645G>C , LRG_130:g.147645G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.1623G>C | ENSP00000484935.2:n.1623G>C | |
| ENST00000504915.3:c.2012G>C | ENSP00000473355.2:p.Arg671Thr | |
| ENST00000505350.2:c.*1964G>C | ENSP00000481752.1:n.*1964G>C | |
| ENST00000507379.6:c.1904G>C | ENSP00000423224.2:p.Arg635Thr | |
| ENST00000509732.6:c.1958G>C | ENSP00000426541.2:p.Arg653Thr | |
| ENST00000512211.7:c.1958G>C | ENSP00000423828.3:p.Arg653Thr | |
| ENST00000257430.9:c.1958G>C MANE Select | ENSP00000257430.4:p.Arg653Thr | |
| ENST00000257430.8:c.1958G>C | ENSP00000257430.4:p.Arg653Thr | |
| ENST00000502371.2:c.311G>C | ||
| ENST00000504915.2:c.647G>C | ENSP00000473355.1:p.Arg216Thr | |
| ENST00000507379.5:c.1904G>C | ENSP00000423224.1:p.Arg635Thr | |
| ENST00000508376.6:c.1958G>C | ENSP00000427089.2:p.Arg653Thr | |
| ENST00000508624.5:c.*1280G>C | ENSP00000424265.1:n.*1280G>C | |
| ENST00000512211.6:c.1958G>C | ENSP00000423828.2:p.Arg653Thr | |
| ENST00000520401.1:c.230+6193G>C | ||
| NM_000038.5:c.1958G>C | NP_000029.2:p.Arg653Thr | |
| NM_001127510.2:c.1958G>C | NP_001120982.1:p.Arg653Thr | |
| NM_001127511.2:c.1904G>C | NP_001120983.2:p.Arg635Thr | |
| NM_001354895.1:c.1958G>C | NP_001341824.1:p.Arg653Thr | |
| NM_001354896.1:c.2012G>C | NP_001341825.1:p.Arg671Thr | |
| NM_001354897.1:c.1988G>C | NP_001341826.1:p.Arg663Thr | |
| NM_001354898.1:c.1883G>C | NP_001341827.1:p.Arg628Thr | |
| NM_001354899.1:c.1874G>C | NP_001341828.1:p.Arg625Thr | |
| NM_001354900.1:c.1835G>C | NP_001341829.1:p.Arg612Thr | |
| NM_001354901.1:c.1781G>C | NP_001341830.1:p.Arg594Thr | |
| NM_001354902.1:c.1685G>C | NP_001341831.1:p.Arg562Thr | |
| NM_001354903.1:c.1655G>C | NP_001341832.1:p.Arg552Thr | |
| NM_001354904.1:c.1580G>C | NP_001341833.1:p.Arg527Thr | |
| NM_001354905.1:c.1478G>C | NP_001341834.1:p.Arg493Thr | |
| NM_001354906.1:c.1109G>C | NP_001341835.1:p.Arg370Thr | |
| NM_000038.6:c.1958G>C MANE Select | NP_000029.2:p.Arg653Thr | |
| NM_001127510.3:c.1958G>C | NP_001120982.1:p.Arg653Thr | |
| NM_001127511.3:c.1904G>C | NP_001120983.2:p.Arg635Thr | |
| NM_001354895.2:c.1958G>C | NP_001341824.1:p.Arg653Thr | |
| NM_001354896.2:c.2012G>C | NP_001341825.1:p.Arg671Thr | |
| NM_001354897.2:c.1988G>C | NP_001341826.1:p.Arg663Thr | |
| NM_001354898.2:c.1883G>C | NP_001341827.1:p.Arg628Thr | |
| NM_001354899.2:c.1874G>C | NP_001341828.1:p.Arg625Thr | |
| NM_001354900.2:c.1835G>C | NP_001341829.1:p.Arg612Thr | |
| NM_001354901.2:c.1781G>C | NP_001341830.1:p.Arg594Thr | |
| NM_001354902.2:c.1685G>C | NP_001341831.1:p.Arg562Thr | |
| NM_001354903.2:c.1655G>C | NP_001341832.1:p.Arg552Thr | |
| NM_001354904.2:c.1580G>C | NP_001341833.1:p.Arg527Thr | |
| NM_001354905.2:c.1478G>C | NP_001341834.1:p.Arg493Thr | |
| NM_001354906.2:c.1109G>C | NP_001341835.1:p.Arg370Thr |