Linked Data
ClinVar Variation Id:
1209778
dbSNP Id:
rs148131756
ExAC:
1:46660026 G / A
gnomAD v2:
1-46660026-G-A
gnomAD v4:
1-46194354-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.46194354G>A , CM000663.2:g.46194354G>A | GRCh38 |
| NC_000001.10:g.46660026G>A , CM000663.1:g.46660026G>A | GRCh37 |
| NC_000001.9:g.46432613G>A | NCBI36 |
| NG_009205.2:g.30952C>T | |
| NG_009205.3:g.30952C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000396420.8:c.799C>T (POMGNT1) | ENSP00000379698.4:p.Arg267Cys | |
| ENST00000477114.2:n.971C>T (POMGNT1) | ||
| ENST00000497439.6:n.971C>T (POMGNT1) | ||
| ENST00000684817.1:n.1159C>T (POMGNT1) | ||
| ENST00000684898.1:n.971C>T (POMGNT1) | ||
| ENST00000685230.1:c.*78C>T (POMGNT1) | ENSP00000510305.1:n.*78C>T | |
| ENST00000685275.1:n.956C>T (POMGNT1) | ||
| ENST00000685444.1:c.700C>T (POMGNT1) | ENSP00000510762.1:p.Arg234Cys | |
| ENST00000685704.1:n.971C>T (POMGNT1) | ||
| ENST00000685775.1:n.1936C>T (POMGNT1) | ||
| ENST00000685833.1:n.1287C>T (POMGNT1) | ||
| ENST00000686252.1:n.1873C>T (POMGNT1) | ||
| ENST00000686379.1:c.799C>T (POMGNT1) | ENSP00000508913.1:p.Arg267Cys | |
| ENST00000686724.1:n.971C>T (POMGNT1) | ||
| ENST00000686737.1:c.799C>T (POMGNT1) | ENSP00000508736.1:p.Arg267Cys | |
| ENST00000687112.1:n.971C>T (POMGNT1) | ||
| ENST00000687149.1:c.799C>T (POMGNT1) | ENSP00000509745.1:p.Arg267Cys | |
| ENST00000687197.1:c.799C>T (POMGNT1) | ENSP00000510749.1:p.Arg267Cys | |
| ENST00000687235.1:n.971C>T (POMGNT1) | ||
| ENST00000687613.1:n.1159C>T (POMGNT1) | ||
| ENST00000687683.1:c.799C>T (POMGNT1) | ENSP00000508522.1:p.Arg267Cys | |
| ENST00000688032.1:n.971C>T (POMGNT1) | ||
| ENST00000688596.1:n.971C>T (POMGNT1) | ||
| ENST00000688608.1:c.700C>T (POMGNT1) | ENSP00000508890.1:p.Arg234Cys | |
| ENST00000688919.1:n.1605C>T (POMGNT1) | ||
| ENST00000689031.1:n.971C>T (POMGNT1) | ||
| ENST00000689717.1:n.971C>T (POMGNT1) | ||
| ENST00000689756.1:c.*431C>T (POMGNT1) | ENSP00000509023.1:n.*431C>T | |
| ENST00000690377.1:n.971C>T (POMGNT1) | ||
| ENST00000690678.1:c.799C>T (POMGNT1) | ENSP00000508703.1:p.Arg267Cys | |
| ENST00000691209.1:c.799C>T (POMGNT1) | ENSP00000510112.1:p.Arg267Cys | |
| ENST00000691243.1:c.799C>T (POMGNT1) | ENSP00000510654.1:p.Arg267Cys | |
| ENST00000692169.1:n.971C>T (POMGNT1) | ||
| ENST00000692202.1:n.1159C>T (POMGNT1) | ||
| ENST00000692322.1:c.*651C>T (POMGNT1) | ENSP00000509017.1:n.*651C>T | |
| ENST00000692369.1:c.799C>T (POMGNT1) | ENSP00000508453.1:p.Arg267Cys | |
| ENST00000692599.1:n.971C>T (POMGNT1) | ||
| ENST00000692635.1:c.799C>T (POMGNT1) | ENSP00000508425.1:p.Arg267Cys | |
| ENST00000693168.1:n.971C>T (POMGNT1) | ||
| ENST00000693218.1:c.799C>T (POMGNT1) | ENSP00000510577.1:p.Arg267Cys | |
| ENST00000693223.1:n.1443C>T (POMGNT1) | ||
| ENST00000693365.1:n.2739C>T (POMGNT1) | ||
| ENST00000371984.8:c.799C>T (POMGNT1) MANE Select | ENSP00000361052.3:p.Arg267Cys | |
| ENST00000371984.7:c.799C>T (POMGNT1) | ENSP00000361052.3:p.Arg267Cys | |
| ENST00000371992.1:c.799C>T (POMGNT1) | ENSP00000361060.1:p.Arg267Cys | |
| ENST00000396420.7:c.*78C>T (POMGNT1) | ENSP00000379698.3:n.*78C>T | |
| ENST00000477114.1:n.147C>T (POMGNT1) | ||
| NM_001243766.1:c.799C>T (POMGNT1) | NP_001230695.1:p.Arg267Cys | |
| NM_001290129.1:c.733C>T (POMGNT1) | NP_001277058.1:p.Arg245Cys | |
| NM_001290130.1:c.370C>T (POMGNT1) | NP_001277059.1:p.Arg124Cys | |
| NM_017739.3:c.799C>T (POMGNT1) | NP_060209.3:p.Arg267Cys | |
| XM_005271010.1:c.799C>T (POMGNT1) | XP_005271067.1:p.Arg267Cys | |
| XM_006710755.1:c.799C>T (POMGNT1) | XP_006710818.1:p.Arg267Cys | |
| XM_006710756.1:c.799C>T (POMGNT1) | XP_006710819.1:p.Arg267Cys | |
| XM_011540460.1:c.679-1848G>A (TSPAN1) | XP_011538762.1:n.679-1848G>A | |
| XM_011540461.1:c.634-1848G>A (TSPAN1) | XP_011538763.1:n.634-1848G>A | |
| XM_011541759.1:c.733C>T (POMGNT1) | XP_011540061.1:p.Arg245Cys | |
| XM_011541760.1:c.733C>T (POMGNT1) | XP_011540062.1:p.Arg245Cys | |
| XM_011541761.1:c.-295C>T (POMGNT1) | XP_011540063.1:n.-295C>T | |
| XR_946706.1:n.958C>T (POMGNT1) | ||
| XM_011540460.3:c.679-1848G>A (TSPAN1) | XP_011538762.1:n.679-1848G>A | |
| XM_011541760.3:c.733C>T (POMGNT1) | XP_011540062.1:p.Arg245Cys | |
| XM_017001690.1:c.799C>T (POMGNT1) | XP_016857179.1:p.Arg267Cys | |
| NM_001243766.2:c.799C>T (POMGNT1) | NP_001230695.2:p.Arg267Cys | |
| NM_001290129.2:c.733C>T (POMGNT1) | NP_001277058.2:p.Arg245Cys | |
| NM_001290130.2:c.370C>T (POMGNT1) | NP_001277059.2:p.Arg124Cys | |
| NM_017739.4:c.799C>T (POMGNT1) MANE Select | NP_060209.4:p.Arg267Cys |