Linked Data
ClinVar Variation Id:
725815
ClinVar RCV Id:
RCV000899935
dbSNP Id:
rs778017231
ExAC:
17:78187661 G / T
gnomAD v2:
17-78187661-G-T
gnomAD v4:
17-80213862-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.80213862G>T , CM000679.2:g.80213862G>T | GRCh38 |
| NC_000017.10:g.78187661G>T , CM000679.1:g.78187661G>T | GRCh37 |
| NC_000017.9:g.75802256G>T | NCBI36 |
| NG_008229.1:g.11539C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703570.1:n.2845-2004G>T (CARD14) | ||
| ENST00000326317.11:c.687C>A (SGSH) MANE Select | ENSP00000314606.6:p.Thr229= | |
| ENST00000326317.10:c.687C>A (SGSH) | ENSP00000314606.6:p.Thr229= | |
| ENST00000570923.1:c.722C>A (SGSH) | ENSP00000458200.1:p.Pro241His | |
| ENST00000572208.5:n.554C>A (SGSH) | ||
| ENST00000572257.5:c.289C>A (SGSH) | ||
| ENST00000573150.5:c.581C>A (SGSH) | ENSP00000459280.1:p.Pro194His | |
| ENST00000574505.5:c.546C>A (SGSH) | ||
| ENST00000575282.5:n.982C>A (SGSH) | ||
| ENST00000576941.5:c.*103C>A (SGSH) | ENSP00000461160.1:n.*103C>A | |
| NM_000199.3:c.687C>A (SGSH) | NP_000190.1:p.Thr229= | |
| XM_005257582.2:c.687C>A (SGSH) | XP_005257639.1:p.Thr229= | |
| XM_005257583.3:c.687C>A (SGSH) | XP_005257640.1:p.Thr229= | |
| XM_011525126.1:c.687C>A (SGSH) | XP_011523428.1:p.Thr229= | |
| XM_011525127.1:c.687C>A (SGSH) | XP_011523429.1:p.Thr229= | |
| XR_934532.1:n.707C>A (SGSH) | ||
| NM_000199.4:c.687C>A (SGSH) | NP_000190.1:p.Thr229= | |
| NM_001352921.1:c.687C>A (SGSH) | NP_001339850.1:p.Thr229= | |
| NM_001352922.1:c.687C>A (SGSH) | NP_001339851.1:p.Thr229= | |
| NR_148201.1:n.668C>A (SGSH) | ||
| XM_005257583.4:c.687C>A (SGSH) | XP_005257640.1:p.Thr229= | |
| XM_017024952.1:c.687C>A (SGSH) | XP_016880441.1:p.Thr229= | |
| XR_001752585.1:n.707C>A (SGSH) | ||
| XR_001752586.1:n.707C>A (SGSH) | ||
| XR_001752587.1:n.707C>A (SGSH) | ||
| XR_001752588.1:n.707C>A (SGSH) | ||
| XR_001752589.1:n.707C>A (SGSH) | ||
| XR_001752590.1:n.707C>A (SGSH) | ||
| XR_001752591.1:n.707C>A (SGSH) | ||
| XR_001752592.1:n.707C>A (SGSH) | ||
| XR_002958057.1:n.707C>A (SGSH) | ||
| XR_934532.2:n.707C>A (SGSH) | ||
| NM_000199.5:c.687C>A (SGSH) MANE Select | NP_000190.1:p.Thr229= | |
| NM_001352921.2:c.687C>A (SGSH) | NP_001339850.1:p.Thr229= | |
| NM_001352922.2:c.687C>A (SGSH) | NP_001339851.1:p.Thr229= | |
| NR_148201.2:n.601C>A (SGSH) | ||
| NM_001352921.3:c.687C>A (SGSH) | NP_001339850.1:p.Thr229= |