Linked Data
dbSNP Id:
rs756847619
ExAC:
1:46655523 C / A
gnomAD v2:
1-46655523-C-A
gnomAD v4:
1-46189851-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.46189851C>A , CM000663.2:g.46189851C>A | GRCh38 |
| NC_000001.10:g.46655523C>A , CM000663.1:g.46655523C>A | GRCh37 |
| NC_000001.9:g.46428110C>A | NCBI36 |
| NG_009205.2:g.35455G>T | |
| NG_009205.3:g.35455G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000396420.8:c.1785+3G>T (POMGNT1) | ENSP00000379698.4:n.1785+3G>T | |
| ENST00000497439.6:n.1957+3G>T (POMGNT1) | ||
| ENST00000684817.1:n.2145+3G>T (POMGNT1) | ||
| ENST00000684898.1:n.2347+3G>T (POMGNT1) | ||
| ENST00000685230.1:c.*1095+3G>T (POMGNT1) | ENSP00000510305.1:n.*1095+3G>T | |
| ENST00000685275.1:n.2332+3G>T (POMGNT1) | ||
| ENST00000685444.1:c.1686+3G>T (POMGNT1) | ENSP00000510762.1:n.1686+3G>T | |
| ENST00000685704.1:n.2451+3G>T (POMGNT1) | ||
| ENST00000685833.1:n.4178+3G>T (POMGNT1) | ||
| ENST00000686252.1:n.2859+3G>T (POMGNT1) | ||
| ENST00000686379.1:c.*909+3G>T (POMGNT1) | ENSP00000508913.1:n.*909+3G>T | |
| ENST00000686724.1:n.3472+3G>T (POMGNT1) | ||
| ENST00000686737.1:c.1785+3G>T (POMGNT1) | ENSP00000508736.1:n.1785+3G>T | |
| ENST00000687112.1:n.2651+3G>T (POMGNT1) | ||
| ENST00000687149.1:c.1824+3G>T (POMGNT1) | ENSP00000509745.1:n.1824+3G>T | |
| ENST00000687197.1:c.*725+3G>T (POMGNT1) | ENSP00000510749.1:n.*725+3G>T | |
| ENST00000687235.1:n.3862+3G>T (POMGNT1) | ||
| ENST00000687613.1:n.2425+3G>T (POMGNT1) | ||
| ENST00000687683.1:c.1785+3G>T (POMGNT1) | ENSP00000508522.1:n.1785+3G>T | |
| ENST00000688032.1:n.2322+3G>T (POMGNT1) | ||
| ENST00000688596.1:n.2436+3G>T (POMGNT1) | ||
| ENST00000688608.1:c.1686+3G>T (POMGNT1) | ENSP00000508890.1:n.1686+3G>T | |
| ENST00000689031.1:n.2237+3G>T (POMGNT1) | ||
| ENST00000689756.1:c.*1417+3G>T (POMGNT1) | ENSP00000509023.1:n.*1417+3G>T | |
| ENST00000690377.1:n.2132+3G>T (POMGNT1) | ||
| ENST00000690678.1:c.1785+3G>T (POMGNT1) | ENSP00000508703.1:n.1785+3G>T | |
| ENST00000691209.1:c.*725+3G>T (POMGNT1) | ENSP00000510112.1:n.*725+3G>T | |
| ENST00000691243.1:c.*176+3G>T (POMGNT1) | ENSP00000510654.1:n.*176+3G>T | |
| ENST00000692202.1:n.2360+3G>T (POMGNT1) | ||
| ENST00000692322.1:c.*1572+3G>T (POMGNT1) | ENSP00000509017.1:n.*1572+3G>T | |
| ENST00000692369.1:c.1785+3G>T (POMGNT1) | ENSP00000508453.1:n.1785+3G>T | |
| ENST00000692599.1:n.3660+3G>T (POMGNT1) | ||
| ENST00000692635.1:c.*660+3G>T (POMGNT1) | ENSP00000508425.1:n.*660+3G>T | |
| ENST00000693168.1:n.3561+3G>T (POMGNT1) | ||
| ENST00000693218.1:c.*346+3G>T (POMGNT1) | ENSP00000510577.1:n.*346+3G>T | |
| ENST00000693223.1:n.2733+3G>T (POMGNT1) | ||
| ENST00000371984.8:c.1785+3G>T (POMGNT1) MANE Select | ENSP00000361052.3:n.1785+3G>T | |
| ENST00000371984.7:c.1785+3G>T (POMGNT1) | ENSP00000361052.3:n.1785+3G>T | |
| ENST00000371992.1:c.1785+3G>T (POMGNT1) | ENSP00000361060.1:n.1785+3G>T | |
| ENST00000396420.7:c.*1454+3G>T (POMGNT1) | ENSP00000379698.3:n.*1454+3G>T | |
| ENST00000480972.1:n.434+3G>T (POMGNT1) | ||
| NM_001243766.1:c.1785+3G>T (POMGNT1) | NP_001230695.1:n.1785+3G>T | |
| NM_001290129.1:c.1719+3G>T (POMGNT1) | NP_001277058.1:n.1719+3G>T | |
| NM_001290130.1:c.1356+3G>T (POMGNT1) | NP_001277059.1:n.1356+3G>T | |
| NM_017739.3:c.1785+3G>T (POMGNT1) | NP_060209.3:n.1785+3G>T | |
| XM_005271010.1:c.1785+3G>T (POMGNT1) | XP_005271067.1:n.1785+3G>T | |
| XM_006710755.1:c.1785+3G>T (POMGNT1) | XP_006710818.1:n.1785+3G>T | |
| XM_006710756.1:c.1785+3G>T (POMGNT1) | XP_006710819.1:n.1785+3G>T | |
| XM_011540460.1:c.678+4543C>A (TSPAN1) | XP_011538762.1:n.678+4543C>A | |
| XM_011540461.1:c.633+4543C>A (TSPAN1) | XP_011538763.1:n.633+4543C>A | |
| XM_011541759.1:c.1719+3G>T (POMGNT1) | XP_011540061.1:n.1719+3G>T | |
| XM_011541760.1:c.1719+3G>T (POMGNT1) | XP_011540062.1:n.1719+3G>T | |
| XM_011541761.1:c.693+3G>T (POMGNT1) | XP_011540063.1:n.693+3G>T | |
| XM_011540460.3:c.678+4543C>A (TSPAN1) | XP_011538762.1:n.678+4543C>A | |
| XM_011541760.3:c.1719+3G>T (POMGNT1) | XP_011540062.1:n.1719+3G>T | |
| XM_017001690.1:c.1785+3G>T (POMGNT1) | XP_016857179.1:n.1785+3G>T | |
| NM_001243766.2:c.1785+3G>T (POMGNT1) | NP_001230695.2:n.1785+3G>T | |
| NM_001290129.2:c.1719+3G>T (POMGNT1) | NP_001277058.2:n.1719+3G>T | |
| NM_001290130.2:c.1356+3G>T (POMGNT1) | NP_001277059.2:n.1356+3G>T | |
| NM_017739.4:c.1785+3G>T (POMGNT1) MANE Select | NP_060209.4:n.1785+3G>T |