Linked Data
ClinVar Variation Id:
235490
dbSNP Id:
rs141641266
ExAC:
11:6415245 C / T
gnomAD v2:
11-6415245-C-T
gnomAD v3:
11-6394015-C-T
gnomAD v4:
11-6394015-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6394015C>T , CM000673.2:g.6394015C>T | GRCh38 |
| NC_000011.9:g.6415245C>T , CM000673.1:g.6415245C>T | GRCh37 |
| NC_000011.8:g.6371821C>T | NCBI36 |
| NG_011780.1:g.8591C>T | |
| NG_029615.1:g.30400G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342245.9:c.1460C>T MANE Select | ENSP00000340409.4:p.Ala487Val | |
| ENST00000342245.8:c.1460C>T | ENSP00000340409.4:p.Ala487Val | |
| ENST00000526280.1:c.517C>T | ||
| ENST00000527275.5:c.1457C>T | ENSP00000435350.1:p.Ala486Val | |
| ENST00000531303.5:c.*291C>T | ENSP00000432625.1:n.*291C>T | |
| ENST00000531336.1:n.292C>T | ||
| ENST00000532367.1:n.296C>T | ||
| ENST00000533123.5:c.*187C>T | ENSP00000435950.1:n.*187C>T | |
| ENST00000534405.5:c.*291C>T | ENSP00000434353.1:n.*291C>T | |
| NM_000543.4:c.1460C>T | NP_000534.3:p.Ala487Val | |
| NM_001007593.2:c.1457C>T | NP_001007594.2:p.Ala486Val | |
| XM_005253075.3:c.1460C>T | XP_005253132.1:p.Ala487Val | |
| XM_011520303.1:c.1328C>T | XP_011518605.1:p.Ala443Val | |
| XM_011520304.1:c.1328C>T | XP_011518606.1:p.Ala443Val | |
| XR_930886.1:n.1798C>T | ||
| NM_001318087.1:c.1460C>T | NP_001305016.1:p.Ala487Val | |
| NM_001318088.1:c.539C>T | NP_001305017.1:p.Ala180Val | |
| NM_001365135.1:c.1328C>T | NP_001352064.1:p.Ala443Val | |
| NR_027400.2:n.1473C>T | ||
| NR_134502.1:n.992C>T | ||
| XM_011520304.2:c.1328C>T | XP_011518606.1:p.Ala443Val | |
| XR_001747940.2:n.1625C>T | ||
| XR_002957158.1:n.1827C>T | ||
| NM_000543.5:c.1460C>T MANE Select | NP_000534.3:p.Ala487Val | |
| NM_001007593.3:c.1457C>T | NP_001007594.2:p.Ala486Val | |
| NM_001318087.2:c.1460C>T | NP_001305016.1:p.Ala487Val | |
| NM_001318088.2:c.539C>T | NP_001305017.1:p.Ala180Val | |
| NM_001365135.2:c.1328C>T | NP_001352064.1:p.Ala443Val | |
| NR_027400.3:n.1413C>T | ||
| NR_134502.2:n.932C>T |