Revel Score:
ENST00000397752 (MANE Select)
0.627
ENST00000318493
0.627
ENST00000539704
0.627
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.116783360A>T , CM000669.2:g.116783360A>T | GRCh38 |
| NC_000007.13:g.116423414A>T , CM000669.1:g.116423414A>T | GRCh37 |
| NC_000007.12:g.116210650A>T | NCBI36 |
| NG_008996.1:g.115956A>T , LRG_662:g.115956A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000436117.3:c.*1294A>T | ENSP00000410980.2:n.*1294A>T | |
| ENST00000318493.11:c.3743A>T | ENSP00000317272.6:p.Tyr1248Phe | |
| ENST00000397752.8:c.3689A>T MANE Select | ENSP00000380860.3:p.Tyr1230Phe | |
| ENST00000318493.10:c.3743A>T | ENSP00000317272.6:p.Tyr1248Phe | |
| ENST00000397752.7:c.3689A>T | ENSP00000380860.3:p.Tyr1230Phe | |
| NM_000245.2:c.3689A>T | NP_000236.2:p.Tyr1230Phe | |
| NM_001127500.1:c.3743A>T , LRG_662t1:c.3743A>T | NP_001120972.1:p.Tyr1248Phe | |
| XM_006715990.2:c.2399A>T | XP_006716053.1:p.Tyr800Phe | |
| XM_006715991.2:c.2399A>T | XP_006716054.1:p.Tyr800Phe | |
| XM_011516223.1:c.3746A>T | XP_011514525.1:p.Tyr1249Phe | |
| NM_000245.3:c.3689A>T | NP_000236.2:p.Tyr1230Phe | |
| NM_001127500.2:c.3743A>T | NP_001120972.1:p.Tyr1248Phe | |
| NM_001324402.1:c.2399A>T | NP_001311331.1:p.Tyr800Phe | |
| XR_001744772.1:n.3820A>T | ||
| NM_001127500.3:c.3743A>T | NP_001120972.1:p.Tyr1248Phe | |
| NM_000245.4:c.3689A>T MANE Select | NP_000236.2:p.Tyr1230Phe | |
| NM_001324402.2:c.2399A>T | NP_001311331.1:p.Tyr800Phe |