Revel Score:
ENST00000543138
0.207
ENST00000370132 (MANE Select)
0.207
gnomAD v3:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.100206504T>A , CM000663.2:g.100206504T>A | GRCh38 |
| NC_000001.10:g.100672060T>A , CM000663.1:g.100672060T>A | GRCh37 |
| NC_000001.9:g.100444648T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000681617.1:c.1276A>T | ENSP00000505544.1:p.Ser426Cys | |
| ENST00000681780.1:c.607A>T | ENSP00000505780.1:p.Ser203Cys | |
| ENST00000370132.8:c.1150A>T MANE Select | ENSP00000359151.3:p.Ser384Cys | |
| XM_005270545.2:c.607A>T | XP_005270602.1:p.Ser203Cys | |
| XM_005270546.2:c.607A>T | XP_005270603.1:p.Ser203Cys | |
| XM_005270545.4:c.607A>T | XP_005270602.1:p.Ser203Cys | |
| XM_017000468.2:c.607A>T | XP_016855957.1:p.Ser203Cys | |
| XM_017000469.2:c.607A>T | XP_016855958.1:p.Ser203Cys | |
| NM_001918.5:c.1150A>T MANE Select | NP_001909.4:p.Ser384Cys | |
| NM_001399969.1:c.607A>T | NP_001386898.1:p.Ser203Cys | |
| NM_001399972.1:c.607A>T | NP_001386901.1:p.Ser203Cys | |
| NR_174363.1:n.982A>T | ||
| NR_174364.1:n.1164A>T | ||
| NR_174365.1:n.947A>T | ||
| NR_174366.1:n.1249A>T |