Linked Data
ClinVar Variation Id:
21474
dbSNP Id:
rs367543041
gnomAD v2:
1-11082610-G-A
gnomAD v4:
1-11022553-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11022553G>A , CM000663.2:g.11022553G>A | GRCh38 |
| NC_000001.10:g.11082610G>A , CM000663.1:g.11082610G>A | GRCh37 |
| NC_000001.9:g.11005197G>A | NCBI36 |
| NG_008734.1:g.14932G>A , LRG_659:g.14932G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700088.1:c.1397-360C>T (MASP2) | ENSP00000514787.1:n.1397-360C>T | |
| ENST00000240185.8:c.1144G>A (TARDBP) MANE Select | ENSP00000240185.4:p.Ala382Thr | |
| ENST00000639083.1:c.1144G>A (TARDBP) | ENSP00000491203.1:p.Ala382Thr | |
| ENST00000639599.1:c.832+312G>A (TARDBP) | ENSP00000492196.1:n.832+312G>A | |
| ENST00000649624.1:c.768+376G>A (TARDBP) | ENSP00000497327.1:n.768+376G>A | |
| ENST00000240185.7:c.1144G>A (TARDBP) | ENSP00000240185.3:p.Ala382Thr | |
| ENST00000315091.7:c.832+312G>A (TARDBP) | ENSP00000313129.3:n.832+312G>A | |
| ENST00000439080.6:c.*725G>A (TARDBP) | ENSP00000404666.3:n.*725G>A | |
| ENST00000473869.5:c.841+303G>A (TARDBP) | ENSP00000432132.1:n.841+303G>A | |
| ENST00000477447.6:c.140+303G>A (TARDBP) | ||
| ENST00000610369.4:c.319+303G>A (TARDBP) | ENSP00000482559.1:n.319+303G>A | |
| ENST00000611136.4:c.212+312G>A | ||
| ENST00000611963.4:c.472+312G>A (TARDBP) | ENSP00000481330.1:n.472+312G>A | |
| ENST00000612542.1:c.107+303G>A | ||
| ENST00000614494.1:c.221+376G>A (TARDBP) | ||
| ENST00000614757.4:c.841+303G>A | ENSP00000481867.1:n.841+303G>A | |
| ENST00000616545.4:c.841+303G>A (TARDBP) | ENSP00000484722.1:n.841+303G>A | |
| ENST00000617172.4:c.582+303G>A (TARDBP) | ||
| ENST00000619555.4:c.392+303G>A (TARDBP) | ||
| ENST00000620505.1:c.246G>A (TARDBP) | ||
| ENST00000620632.4:c.392+303G>A (TARDBP) | ||
| ENST00000621573.1:c.6G>A (TARDBP) | ||
| ENST00000621790.4:c.859+285G>A (TARDBP) | ENSP00000482191.1:n.859+285G>A | |
| ENST00000622057.4:c.579+312G>A (TARDBP) | ||
| ENST00000629725.2:c.841+303G>A (TARDBP) | ENSP00000486989.1:n.841+303G>A | |
| NM_007375.3:c.1144G>A , LRG_659t1:c.1144G>A (TARDBP) | NP_031401.1:p.Ala382Thr | |
| XR_946596.1:n.1266G>A (TARDBP) | ||
| XR_946597.1:n.1266G>A (TARDBP) | ||
| XM_017000863.2:c.1144G>A (TARDBP) | XP_016856352.1:p.Ala382Thr | |
| XM_017000864.2:c.1144G>A (TARDBP) | XP_016856353.1:p.Ala382Thr | |
| XM_017000865.2:c.1144G>A (TARDBP) | XP_016856354.1:p.Ala382Thr | |
| XM_017000866.2:c.1144G>A (TARDBP) | XP_016856355.1:p.Ala382Thr | |
| XM_017000867.2:c.1144G>A (TARDBP) | XP_016856356.1:p.Ala382Thr | |
| XM_017000868.2:c.1144G>A (TARDBP) | XP_016856357.1:p.Ala382Thr | |
| NM_007375.4:c.1144G>A (TARDBP) MANE Select | NP_031401.1:p.Ala382Thr |