Linked Data
ClinVar Variation Id:
848759
ClinVar RCV Id:
RCV001052584
dbSNP Id:
rs761200006
ExAC:
15:91354585 C / T
gnomAD v2:
15-91354585-C-T
gnomAD v4:
15-90811355-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.90811355C>T , CM000677.2:g.90811355C>T | GRCh38 |
| NC_000015.9:g.91354585C>T , CM000677.1:g.91354585C>T | GRCh37 |
| NC_000015.8:g.89155589C>T | NCBI36 |
| NG_007272.1:g.98984C>T , LRG_20:g.98984C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355112.8:c.4025C>T MANE Select | ENSP00000347232.3:p.Ser1342Phe | |
| ENST00000560559.2:n.2598C>T | ||
| ENST00000648453.1:c.4025C>T | ENSP00000497646.1:p.Ser1342Phe | |
| ENST00000680772.1:c.4025C>T | ENSP00000506117.1:p.Ser1342Phe | |
| ENST00000681142.1:c.4025C>T | ENSP00000506682.1:p.Ser1342Phe | |
| ENST00000355112.7:c.4025C>T | ENSP00000347232.3:p.Ser1342Phe | |
| ENST00000558825.5:n.1372C>T | ||
| ENST00000559724.5:c.*2949C>T | ENSP00000453359.1:n.*2949C>T | |
| ENST00000560509.5:c.3632C>T | ENSP00000454158.1:p.Ser1211Phe | |
| ENST00000560821.1:n.445C>T | ||
| NM_000057.3:c.4025C>T | NP_000048.1:p.Ser1342Phe | |
| NM_001287246.1:c.4025C>T | NP_001274175.1:p.Ser1342Phe | |
| NM_001287247.1:c.3632C>T | NP_001274176.1:p.Ser1211Phe | |
| NM_001287248.1:c.2900C>T | NP_001274177.1:p.Ser967Phe | |
| XM_006720632.2:c.2063C>T | XP_006720695.1:p.Ser688Phe | |
| XM_011521881.1:c.2711C>T | XP_011520183.1:p.Ser904Phe | |
| XM_011521881.2:c.2711C>T | XP_011520183.1:p.Ser904Phe | |
| NM_000057.4:c.4025C>T MANE Select | NP_000048.1:p.Ser1342Phe | |
| NM_001287246.2:c.4025C>T | NP_001274175.1:p.Ser1342Phe | |
| NM_001287247.2:c.3632C>T | NP_001274176.1:p.Ser1211Phe | |
| NM_001287248.2:c.2900C>T | NP_001274177.1:p.Ser967Phe |