Revel Score:
ENST00000330883
0.912
ENST00000392968
0.912
ENST00000262186 (MANE Select)
0.912
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150948866T>G , CM000669.2:g.150948866T>G | GRCh38 |
| NC_000007.13:g.150645954T>G , CM000669.1:g.150645954T>G | GRCh37 |
| NC_000007.12:g.150276887T>G | NCBI36 |
| NG_008916.1:g.34061A>C , LRG_288:g.34061A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684241.1:n.3415A>C | ||
| ENST00000262186.10:c.2582A>C MANE Select | ENSP00000262186.5:p.Asn861Thr | |
| ENST00000330883.9:c.1562A>C | ENSP00000328531.4:p.Asn521Thr | |
| ENST00000262186.9:c.2582A>C | ENSP00000262186.5:p.Asn861Thr | |
| ENST00000330883.8:c.1562A>C | ENSP00000328531.4:p.Asn521Thr | |
| NM_000238.3:c.2582A>C , LRG_288t1:c.2582A>C | NP_000229.1:p.Asn861Thr | |
| NM_172057.2:c.1562A>C , LRG_288t3:c.1562A>C | NP_742054.1:p.Asn521Thr | |
| XM_011516185.1:c.2282A>C | XP_011514487.1:p.Asn761Thr | |
| XM_011516186.1:c.2582A>C | XP_011514488.1:p.Asn861Thr | |
| XM_011516185.2:c.2282A>C | XP_011514487.1:p.Asn761Thr | |
| XM_011516186.3:c.2582A>C | XP_011514488.1:p.Asn861Thr | |
| XM_017012195.1:c.2432A>C | XP_016867684.1:p.Asn811Thr | |
| XM_017012196.1:c.2405A>C | XP_016867685.1:p.Asn802Thr | |
| NM_000238.4:c.2582A>C MANE Select | NP_000229.1:p.Asn861Thr | |
| NM_172057.3:c.1562A>C | NP_742054.1:p.Asn521Thr |