Revel Score:
ENST00000457016
0.583
ENST00000257430 (MANE Select)
0.583
ENST00000508376
0.583
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112839825A>G , CM000667.2:g.112839825A>G | GRCh38 |
| NC_000005.9:g.112175522A>G , CM000667.1:g.112175522A>G | GRCh37 |
| NC_000005.8:g.112203421A>G | NCBI36 |
| NG_008481.4:g.152305A>G , LRG_130:g.152305A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.3896A>G | ENSP00000484935.2:n.3896A>G | |
| ENST00000504915.3:c.4285A>G | ENSP00000473355.2:p.Ser1429Gly | |
| ENST00000505350.2:c.*4237A>G | ENSP00000481752.1:n.*4237A>G | |
| ENST00000507379.6:c.4177A>G | ENSP00000423224.2:p.Ser1393Gly | |
| ENST00000509732.6:c.4231A>G | ENSP00000426541.2:p.Ser1411Gly | |
| ENST00000512211.7:c.4231A>G | ENSP00000423828.3:p.Ser1411Gly | |
| ENST00000257430.9:c.4231A>G MANE Select | ENSP00000257430.4:p.Ser1411Gly | |
| ENST00000257430.8:c.4231A>G | ENSP00000257430.4:p.Ser1411Gly | |
| ENST00000502371.2:c.2584A>G | ||
| ENST00000508376.6:c.4231A>G | ENSP00000427089.2:p.Ser1411Gly | |
| ENST00000508624.5:c.*3553A>G | ENSP00000424265.1:n.*3553A>G | |
| ENST00000520401.1:c.230+10853A>G | ||
| NM_000038.5:c.4231A>G | NP_000029.2:p.Ser1411Gly | |
| NM_001127510.2:c.4231A>G | NP_001120982.1:p.Ser1411Gly | |
| NM_001127511.2:c.4177A>G | NP_001120983.2:p.Ser1393Gly | |
| NM_001354895.1:c.4231A>G | NP_001341824.1:p.Ser1411Gly | |
| NM_001354896.1:c.4285A>G | NP_001341825.1:p.Ser1429Gly | |
| NM_001354897.1:c.4261A>G | NP_001341826.1:p.Ser1421Gly | |
| NM_001354898.1:c.4156A>G | NP_001341827.1:p.Ser1386Gly | |
| NM_001354899.1:c.4147A>G | NP_001341828.1:p.Ser1383Gly | |
| NM_001354900.1:c.4108A>G | NP_001341829.1:p.Ser1370Gly | |
| NM_001354901.1:c.4054A>G | NP_001341830.1:p.Ser1352Gly | |
| NM_001354902.1:c.3958A>G | NP_001341831.1:p.Ser1320Gly | |
| NM_001354903.1:c.3928A>G | NP_001341832.1:p.Ser1310Gly | |
| NM_001354904.1:c.3853A>G | NP_001341833.1:p.Ser1285Gly | |
| NM_001354905.1:c.3751A>G | NP_001341834.1:p.Ser1251Gly | |
| NM_001354906.1:c.3382A>G | NP_001341835.1:p.Ser1128Gly | |
| NM_000038.6:c.4231A>G MANE Select | NP_000029.2:p.Ser1411Gly | |
| NM_001127510.3:c.4231A>G | NP_001120982.1:p.Ser1411Gly | |
| NM_001127511.3:c.4177A>G | NP_001120983.2:p.Ser1393Gly | |
| NM_001354895.2:c.4231A>G | NP_001341824.1:p.Ser1411Gly | |
| NM_001354896.2:c.4285A>G | NP_001341825.1:p.Ser1429Gly | |
| NM_001354897.2:c.4261A>G | NP_001341826.1:p.Ser1421Gly | |
| NM_001354898.2:c.4156A>G | NP_001341827.1:p.Ser1386Gly | |
| NM_001354899.2:c.4147A>G | NP_001341828.1:p.Ser1383Gly | |
| NM_001354900.2:c.4108A>G | NP_001341829.1:p.Ser1370Gly | |
| NM_001354901.2:c.4054A>G | NP_001341830.1:p.Ser1352Gly | |
| NM_001354902.2:c.3958A>G | NP_001341831.1:p.Ser1320Gly | |
| NM_001354903.2:c.3928A>G | NP_001341832.1:p.Ser1310Gly | |
| NM_001354904.2:c.3853A>G | NP_001341833.1:p.Ser1285Gly | |
| NM_001354905.2:c.3751A>G | NP_001341834.1:p.Ser1251Gly | |
| NM_001354906.2:c.3382A>G | NP_001341835.1:p.Ser1128Gly |