Linked Data
ClinVar Variation Id:
577847
ClinVar RCV Id:
RCV000700696
dbSNP Id:
rs150222010
ExAC:
17:78184501 G / A
gnomAD v2:
17-78184501-G-A
gnomAD v3:
17-80210702-G-A
gnomAD v4:
17-80210702-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.80210702G>A , CM000679.2:g.80210702G>A | GRCh38 |
| NC_000017.10:g.78184501G>A , CM000679.1:g.78184501G>A | GRCh37 |
| NC_000017.9:g.75799096G>A | NCBI36 |
| NG_008229.1:g.14699C>T | |
| NG_032778.1:g.45711G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703570.1:n.2844+1444G>A (CARD14) | ||
| ENST00000326317.11:c.1259C>T (SGSH) MANE Select | ENSP00000314606.6:p.Pro420Leu | |
| ENST00000326317.10:c.1259C>T (SGSH) | ENSP00000314606.6:p.Pro420Leu | |
| ENST00000572257.5:c.551+1369C>T (SGSH) | ||
| ENST00000573150.5:c.*469C>T (SGSH) | ENSP00000459280.1:n.*469C>T | |
| ENST00000575282.5:n.4142C>T (SGSH) | ||
| ENST00000576856.1:c.513C>T (SGSH) | ENSP00000460720.1:n.513C>T | |
| NM_000199.3:c.1259C>T (SGSH) | NP_000190.1:p.Pro420Leu | |
| XM_005257583.3:c.949+1369C>T (SGSH) | XP_005257640.1:n.949+1369C>T | |
| NM_000199.4:c.1259C>T (SGSH) | NP_000190.1:p.Pro420Leu | |
| NM_001352921.1:c.*346C>T (SGSH) | NP_001339850.1:n.*346C>T | |
| NM_001352922.1:c.*309C>T (SGSH) | NP_001339851.1:n.*309C>T | |
| NR_148201.1:n.1240C>T (SGSH) | ||
| XM_005257583.4:c.949+1369C>T (SGSH) | XP_005257640.1:n.949+1369C>T | |
| XM_017024952.1:c.*1163C>T (SGSH) | XP_016880441.1:n.*1163C>T | |
| XR_001752585.1:n.1279C>T (SGSH) | ||
| XR_001752586.1:n.969+1369C>T (SGSH) | ||
| XR_001752587.1:n.969+1369C>T (SGSH) | ||
| XR_001752588.1:n.969+1369C>T (SGSH) | ||
| XR_001752589.1:n.969+1369C>T (SGSH) | ||
| XR_001752590.1:n.969+1369C>T (SGSH) | ||
| XR_001752591.1:n.969+1369C>T (SGSH) | ||
| XR_001752592.1:n.969+1369C>T (SGSH) | ||
| XR_002958057.1:n.1024+1167C>T (SGSH) | ||
| NM_000199.5:c.1259C>T (SGSH) MANE Select | NP_000190.1:p.Pro420Leu | |
| NM_001352921.2:c.*346C>T (SGSH) | NP_001339850.1:n.*346C>T | |
| NM_001352922.2:c.*309C>T (SGSH) | NP_001339851.1:n.*309C>T | |
| NR_148201.2:n.1173C>T (SGSH) | ||
| NM_001352921.3:c.*346C>T (SGSH) | NP_001339850.1:n.*346C>T |