Linked Data
ClinVar Variation Id:
421394
dbSNP Id:
rs1064795109
gnomAD v2:
17-78184331-C-T
gnomAD v3:
17-80210532-C-T
gnomAD v4:
17-80210532-C-T
COSMIC:
COSM3748653
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.80210532C>T , CM000679.2:g.80210532C>T | GRCh38 |
| NC_000017.10:g.78184331C>T , CM000679.1:g.78184331C>T | GRCh37 |
| NC_000017.9:g.75798926C>T | NCBI36 |
| NG_008229.1:g.14869G>A | |
| NG_032778.1:g.45541C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000703570.1:n.2844+1274C>T (CARD14) | ||
| ENST00000326317.11:c.1429G>A (SGSH) MANE Select | ENSP00000314606.6:p.Asp477Asn | |
| ENST00000326317.10:c.1429G>A (SGSH) | ENSP00000314606.6:p.Asp477Asn | |
| ENST00000572257.5:c.551+1539G>A (SGSH) | ||
| ENST00000573150.5:c.*639G>A (SGSH) | ENSP00000459280.1:n.*639G>A | |
| ENST00000575282.5:n.4312G>A (SGSH) | ||
| ENST00000576856.1:c.683G>A (SGSH) | ENSP00000460720.1:n.683G>A | |
| NM_000199.3:c.1429G>A (SGSH) | NP_000190.1:p.Asp477Asn | |
| XM_005257583.3:c.949+1539G>A (SGSH) | XP_005257640.1:n.949+1539G>A | |
| NM_000199.4:c.1429G>A (SGSH) | NP_000190.1:p.Asp477Asn | |
| NM_001352921.1:c.*516G>A (SGSH) | NP_001339850.1:n.*516G>A | |
| NM_001352922.1:c.*479G>A (SGSH) | NP_001339851.1:n.*479G>A | |
| NR_148201.1:n.1410G>A (SGSH) | ||
| XM_005257583.4:c.949+1539G>A (SGSH) | XP_005257640.1:n.949+1539G>A | |
| XM_017024952.1:c.*1333G>A (SGSH) | XP_016880441.1:n.*1333G>A | |
| XR_001752585.1:n.1449G>A (SGSH) | ||
| XR_001752586.1:n.969+1539G>A (SGSH) | ||
| XR_001752587.1:n.969+1539G>A (SGSH) | ||
| XR_001752588.1:n.969+1539G>A (SGSH) | ||
| XR_001752589.1:n.969+1539G>A (SGSH) | ||
| XR_001752590.1:n.969+1539G>A (SGSH) | ||
| XR_001752591.1:n.969+1539G>A (SGSH) | ||
| XR_001752592.1:n.969+1539G>A (SGSH) | ||
| XR_002958057.1:n.1024+1337G>A (SGSH) | ||
| NM_000199.5:c.1429G>A (SGSH) MANE Select | NP_000190.1:p.Asp477Asn | |
| NM_001352921.2:c.*516G>A (SGSH) | NP_001339850.1:n.*516G>A | |
| NM_001352922.2:c.*479G>A (SGSH) | NP_001339851.1:n.*479G>A | |
| NR_148201.2:n.1343G>A (SGSH) | ||
| NM_001352921.3:c.*516G>A (SGSH) | NP_001339850.1:n.*516G>A |