Linked Data
ClinVar Variation Id:
471400
dbSNP Id:
rs183698543
gnomAD v3:
1-46192944-A-G
gnomAD v4:
1-46192944-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.46192944A>G , CM000663.2:g.46192944A>G | GRCh38 |
| NC_000001.10:g.46658616A>G , CM000663.1:g.46658616A>G | GRCh37 |
| NC_000001.9:g.46431203A>G | NCBI36 |
| NG_009205.2:g.32362T>C | |
| NG_009205.3:g.32362T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000396420.8:c.1167T>C (POMGNT1) | ENSP00000379698.4:p.Ala389= | |
| ENST00000477114.2:n.1729T>C (POMGNT1) | ||
| ENST00000497439.6:n.1339T>C (POMGNT1) | ||
| ENST00000684817.1:n.1527T>C (POMGNT1) | ||
| ENST00000684898.1:n.1729T>C (POMGNT1) | ||
| ENST00000685230.1:c.*477T>C (POMGNT1) | ENSP00000510305.1:n.*477T>C | |
| ENST00000685275.1:n.1714T>C (POMGNT1) | ||
| ENST00000685444.1:c.1068T>C (POMGNT1) | ENSP00000510762.1:p.Ala356= | |
| ENST00000685704.1:n.1729T>C (POMGNT1) | ||
| ENST00000685775.1:n.2694T>C (POMGNT1) | ||
| ENST00000685833.1:n.2045T>C (POMGNT1) | ||
| ENST00000686252.1:n.2241T>C (POMGNT1) | ||
| ENST00000686379.1:c.*291T>C (POMGNT1) | ENSP00000508913.1:n.*291T>C | |
| ENST00000686724.1:n.1339T>C (POMGNT1) | ||
| ENST00000686737.1:c.1167T>C (POMGNT1) | ENSP00000508736.1:p.Ala389= | |
| ENST00000687112.1:n.2033T>C (POMGNT1) | ||
| ENST00000687149.1:c.1167T>C (POMGNT1) | ENSP00000509745.1:p.Ala389= | |
| ENST00000687197.1:c.*107T>C (POMGNT1) | ENSP00000510749.1:n.*107T>C | |
| ENST00000687235.1:n.1729T>C (POMGNT1) | ||
| ENST00000687613.1:n.1917T>C (POMGNT1) | ||
| ENST00000687683.1:c.1167T>C (POMGNT1) | ENSP00000508522.1:p.Ala389= | |
| ENST00000688032.1:n.1729T>C (POMGNT1) | ||
| ENST00000688596.1:n.1818T>C (POMGNT1) | ||
| ENST00000688608.1:c.1068T>C (POMGNT1) | ENSP00000508890.1:p.Ala356= | |
| ENST00000688919.1:n.2363T>C (POMGNT1) | ||
| ENST00000689031.1:n.1729T>C (POMGNT1) | ||
| ENST00000689717.1:n.1339T>C (POMGNT1) | ||
| ENST00000689756.1:c.*799T>C (POMGNT1) | ENSP00000509023.1:n.*799T>C | |
| ENST00000690377.1:n.1514T>C (POMGNT1) | ||
| ENST00000690678.1:c.1167T>C (POMGNT1) | ENSP00000508703.1:p.Ala389= | |
| ENST00000691209.1:c.*107T>C (POMGNT1) | ENSP00000510112.1:n.*107T>C | |
| ENST00000691243.1:c.1167T>C (POMGNT1) | ENSP00000510654.1:p.Ala389= | |
| ENST00000692169.1:n.1316T>C (POMGNT1) | ||
| ENST00000692202.1:n.1742T>C (POMGNT1) | ||
| ENST00000692322.1:c.*1019T>C (POMGNT1) | ENSP00000509017.1:n.*1019T>C | |
| ENST00000692369.1:c.1167T>C (POMGNT1) | ENSP00000508453.1:p.Ala389= | |
| ENST00000692599.1:n.1729T>C (POMGNT1) | ||
| ENST00000692635.1:c.*107T>C (POMGNT1) | ENSP00000508425.1:n.*107T>C | |
| ENST00000693168.1:n.1428T>C (POMGNT1) | ||
| ENST00000693218.1:c.1167T>C (POMGNT1) | ENSP00000510577.1:p.Ala389= | |
| ENST00000693223.1:n.2115T>C (POMGNT1) | ||
| ENST00000693365.1:n.3801T>C (POMGNT1) | ||
| ENST00000371984.8:c.1167T>C (POMGNT1) MANE Select | ENSP00000361052.3:p.Ala389= | |
| ENST00000371984.7:c.1167T>C (POMGNT1) | ENSP00000361052.3:p.Ala389= | |
| ENST00000371992.1:c.1167T>C (POMGNT1) | ENSP00000361060.1:p.Ala389= | |
| ENST00000396420.7:c.*836T>C (POMGNT1) | ENSP00000379698.3:n.*836T>C | |
| ENST00000485714.1:n.553T>C (POMGNT1) | ||
| NM_001243766.1:c.1167T>C (POMGNT1) | NP_001230695.1:p.Ala389= | |
| NM_001290129.1:c.1101T>C (POMGNT1) | NP_001277058.1:p.Ala367= | |
| NM_001290130.1:c.738T>C (POMGNT1) | NP_001277059.1:p.Ala246= | |
| NM_017739.3:c.1167T>C (POMGNT1) | NP_060209.3:p.Ala389= | |
| XM_005271010.1:c.1167T>C (POMGNT1) | XP_005271067.1:p.Ala389= | |
| XM_006710755.1:c.1167T>C (POMGNT1) | XP_006710818.1:p.Ala389= | |
| XM_006710756.1:c.1167T>C (POMGNT1) | XP_006710819.1:p.Ala389= | |
| XM_011540460.1:c.679-3258A>G (TSPAN1) | XP_011538762.1:n.679-3258A>G | |
| XM_011540461.1:c.634-3258A>G (TSPAN1) | XP_011538763.1:n.634-3258A>G | |
| XM_011541759.1:c.1101T>C (POMGNT1) | XP_011540061.1:p.Ala367= | |
| XM_011541760.1:c.1101T>C (POMGNT1) | XP_011540062.1:p.Ala367= | |
| XM_011541761.1:c.74T>C (POMGNT1) | XP_011540063.1:p.Leu25Pro | |
| XR_946706.1:n.1326T>C (POMGNT1) | ||
| XM_011540460.3:c.679-3258A>G (TSPAN1) | XP_011538762.1:n.679-3258A>G | |
| XM_011541760.3:c.1101T>C (POMGNT1) | XP_011540062.1:p.Ala367= | |
| XM_017001690.1:c.1167T>C (POMGNT1) | XP_016857179.1:p.Ala389= | |
| NM_001243766.2:c.1167T>C (POMGNT1) | NP_001230695.2:p.Ala389= | |
| NM_001290129.2:c.1101T>C (POMGNT1) | NP_001277058.2:p.Ala367= | |
| NM_001290130.2:c.738T>C (POMGNT1) | NP_001277059.2:p.Ala246= | |
| NM_017739.4:c.1167T>C (POMGNT1) MANE Select | NP_060209.4:p.Ala389= |