Linked Data
ClinVar Variation Id:
383967
dbSNP Id:
rs1057521801
gnomAD v4:
17-80213876-A-G
PubMed:
PMID:21204211
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.80213876A>G , CM000679.2:g.80213876A>G | GRCh38 |
| NC_000017.10:g.78187675A>G , CM000679.1:g.78187675A>G | GRCh37 |
| NC_000017.9:g.75802270A>G | NCBI36 |
| NG_008229.1:g.11525T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000703570.1:n.2845-1990A>G (CARD14) | ||
| ENST00000326317.11:c.673T>C (SGSH) MANE Select | ENSP00000314606.6:p.Phe225Leu | |
| ENST00000326317.10:c.673T>C (SGSH) | ENSP00000314606.6:p.Phe225Leu | |
| ENST00000570923.1:c.708T>C (SGSH) | ENSP00000458200.1:p.Thr236= | |
| ENST00000572208.5:n.540T>C (SGSH) | ||
| ENST00000572257.5:c.275T>C (SGSH) | ||
| ENST00000573150.5:c.567T>C (SGSH) | ENSP00000459280.1:p.Thr189= | |
| ENST00000574505.5:c.532T>C (SGSH) | ||
| ENST00000575282.5:n.968T>C (SGSH) | ||
| ENST00000576941.5:c.*89T>C (SGSH) | ENSP00000461160.1:n.*89T>C | |
| NM_000199.3:c.673T>C (SGSH) | NP_000190.1:p.Phe225Leu | |
| XM_005257582.2:c.673T>C (SGSH) | XP_005257639.1:p.Phe225Leu | |
| XM_005257583.3:c.673T>C (SGSH) | XP_005257640.1:p.Phe225Leu | |
| XM_011525126.1:c.673T>C (SGSH) | XP_011523428.1:p.Phe225Leu | |
| XM_011525127.1:c.673T>C (SGSH) | XP_011523429.1:p.Phe225Leu | |
| XR_934532.1:n.693T>C (SGSH) | ||
| NM_000199.4:c.673T>C (SGSH) | NP_000190.1:p.Phe225Leu | |
| NM_001352921.1:c.673T>C (SGSH) | NP_001339850.1:p.Phe225Leu | |
| NM_001352922.1:c.673T>C (SGSH) | NP_001339851.1:p.Phe225Leu | |
| NR_148201.1:n.654T>C (SGSH) | ||
| XM_005257583.4:c.673T>C (SGSH) | XP_005257640.1:p.Phe225Leu | |
| XM_017024952.1:c.673T>C (SGSH) | XP_016880441.1:p.Phe225Leu | |
| XR_001752585.1:n.693T>C (SGSH) | ||
| XR_001752586.1:n.693T>C (SGSH) | ||
| XR_001752587.1:n.693T>C (SGSH) | ||
| XR_001752588.1:n.693T>C (SGSH) | ||
| XR_001752589.1:n.693T>C (SGSH) | ||
| XR_001752590.1:n.693T>C (SGSH) | ||
| XR_001752591.1:n.693T>C (SGSH) | ||
| XR_001752592.1:n.693T>C (SGSH) | ||
| XR_002958057.1:n.693T>C (SGSH) | ||
| XR_934532.2:n.693T>C (SGSH) | ||
| NM_000199.5:c.673T>C (SGSH) MANE Select | NP_000190.1:p.Phe225Leu | |
| NM_001352921.2:c.673T>C (SGSH) | NP_001339850.1:p.Phe225Leu | |
| NM_001352922.2:c.673T>C (SGSH) | NP_001339851.1:p.Phe225Leu | |
| NR_148201.2:n.587T>C (SGSH) | ||
| NM_001352921.3:c.673T>C (SGSH) | NP_001339850.1:p.Phe225Leu |