Revel Score:
ENST00000374695 (MANE Select)
0.344
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.21880156T>A , CM000663.2:g.21880156T>A | GRCh38 |
| NC_000001.10:g.22206649T>A , CM000663.1:g.22206649T>A | GRCh37 |
| NC_000001.9:g.22079236T>A | NCBI36 |
| NG_016740.1:g.62102A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374695.8:c.2294A>T MANE Select | ENSP00000363827.3:p.Asn765Ile | |
| ENST00000374695.7:c.2294A>T | ENSP00000363827.3:p.Asn765Ile | |
| NM_001291860.1:c.2297A>T | NP_001278789.1:p.Asn766Ile | |
| NM_005529.6:c.2294A>T | NP_005520.4:p.Asn765Ile | |
| XM_006710594.2:c.2345A>T | XP_006710657.1:p.Asn782Ile | |
| XM_006710595.2:c.2297A>T | XP_006710658.1:p.Asn766Ile | |
| XM_006710596.2:c.2348A>T | XP_006710659.1:p.Asn783Ile | |
| XM_006710597.2:c.2294A>T | XP_006710660.1:p.Asn765Ile | |
| XM_011541317.1:c.2348A>T | XP_011539619.1:p.Asn783Ile | |
| XM_011541318.1:c.2348A>T | XP_011539620.1:p.Asn783Ile | |
| XM_011541319.1:c.2348A>T | XP_011539621.1:p.Asn783Ile | |
| XM_011541320.1:c.2348A>T | XP_011539622.1:p.Asn783Ile | |
| XM_011541321.1:c.2348A>T | XP_011539623.1:p.Asn783Ile | |
| XM_011541322.1:c.2348A>T | XP_011539624.1:p.Asn783Ile | |
| XM_011541318.2:c.2348A>T | XP_011539620.1:p.Asn783Ile | |
| XM_017001120.1:c.2489A>T | XP_016856609.1:p.Asn830Ile | |
| XM_017001121.1:c.2438A>T | XP_016856610.1:p.Asn813Ile | |
| XM_017001122.1:c.2435A>T | XP_016856611.1:p.Asn812Ile | |
| NM_005529.7:c.2294A>T MANE Select | NP_005520.4:p.Asn765Ile | |
| NM_001291860.2:c.2297A>T | NP_001278789.1:p.Asn766Ile |