Deletion | NM_000478.6(ALPL):c.1553_1568del (p.Tyr518fs) | ALPL | Pathogenic/Likely pathogenic | 1 | 21904117 | 21904132 | TCTACCCCCTGAGCGTC | T | criteria provided, multiple submitters, no conflicts | - |
Duplication | NM_000478.6(ALPL):c.1017dup (p.His340fs) | ALPL | Pathogenic/Likely pathogenic | 1 | 21902242 | 21902243 | C | CG | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000478.6(ALPL):c.1471G>A (p.Gly491Arg) | ALPL | Pathogenic/Likely pathogenic | 1 | 21904037 | 21904037 | G | A | criteria provided, multiple submitters, no conflicts | - |
Deletion | NM_000478.6(ALPL):c.963del (p.Lys322fs) | ALPL | Likely pathogenic | 1 | 21900257 | 21900257 | CG | C | criteria provided, single submitter | - |
single nucleotide variant | NM_000478.6(ALPL):c.1171C>T (p.Arg391Cys) | ALPL | Pathogenic/Likely pathogenic | 1 | 21902399 | 21902399 | C | T | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000478.6(ALPL):c.994G>T (p.Glu332Ter) | ALPL | Pathogenic | 1 | 21900289 | 21900289 | G | T | criteria provided, single submitter | - |
single nucleotide variant | NM_000478.6(ALPL):c.395C>T (p.Ala132Val) | ALPL | Likely pathogenic | 1 | 21889700 | 21889700 | C | T | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000478.6(ALPL):c.1142A>G (p.His381Arg) | ALPL | Pathogenic/Likely pathogenic | 1 | 21902370 | 21902370 | A | G | criteria provided, multiple submitters, no conflicts | - |
Duplication | NM_000478.6(ALPL):c.1182dup (p.Ile395fs) | ALPL | Pathogenic/Likely pathogenic | 1 | 21902409 | 21902410 | C | CT | criteria provided, multiple submitters, no conflicts | - |
Deletion | NM_000478.6(ALPL):c.1474del (p.Ala492fs) | ALPL | Pathogenic | 1 | 21904037 | 21904037 | CG | C | criteria provided, multiple submitters, no conflicts | - |