Linked Data
ClinVar Variation Id:
198222
ClinVar RCV Id:
RCV000179495
RCV000263792
RCV000356295
RCV000724803
RCV001081913
RCV001277259
RCV004539682
dbSNP Id:
rs189274856
ExAC:
1:46661603 G / T
gnomAD v2:
1-46661603-G-T
gnomAD v3:
1-46195931-G-T
gnomAD v4:
1-46195931-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.46195931G>T , CM000663.2:g.46195931G>T | GRCh38 |
| NC_000001.10:g.46661603G>T , CM000663.1:g.46661603G>T | GRCh37 |
| NC_000001.9:g.46434190G>T | NCBI36 |
| NG_009205.2:g.29375C>A | |
| NG_009205.3:g.29375C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000396420.8:c.421-7C>A (POMGNT1) | ENSP00000379698.4:n.421-7C>A | |
| ENST00000477114.2:n.593-7C>A (POMGNT1) | ||
| ENST00000497439.6:n.593-7C>A (POMGNT1) | ||
| ENST00000684817.1:n.589-7C>A (POMGNT1) | ||
| ENST00000684898.1:n.593-7C>A (POMGNT1) | ||
| ENST00000685230.1:c.421-7C>A (POMGNT1) | ENSP00000510305.1:n.421-7C>A | |
| ENST00000685275.1:n.578-7C>A (POMGNT1) | ||
| ENST00000685444.1:c.421-7C>A (POMGNT1) | ENSP00000510762.1:n.421-7C>A | |
| ENST00000685704.1:n.593-7C>A (POMGNT1) | ||
| ENST00000685775.1:n.1366-7C>A (POMGNT1) | ||
| ENST00000685833.1:n.566-7C>A (POMGNT1) | ||
| ENST00000686252.1:n.1495-7C>A (POMGNT1) | ||
| ENST00000686379.1:c.421-7C>A (POMGNT1) | ENSP00000508913.1:n.421-7C>A | |
| ENST00000686724.1:n.593-7C>A (POMGNT1) | ||
| ENST00000686737.1:c.421-7C>A (POMGNT1) | ENSP00000508736.1:n.421-7C>A | |
| ENST00000687112.1:n.593-7C>A (POMGNT1) | ||
| ENST00000687149.1:c.421-7C>A (POMGNT1) | ENSP00000509745.1:n.421-7C>A | |
| ENST00000687197.1:c.421-7C>A (POMGNT1) | ENSP00000510749.1:n.421-7C>A | |
| ENST00000687235.1:n.593-7C>A (POMGNT1) | ||
| ENST00000687613.1:n.589-7C>A (POMGNT1) | ||
| ENST00000687683.1:c.421-7C>A (POMGNT1) | ENSP00000508522.1:n.421-7C>A | |
| ENST00000688032.1:n.593-7C>A (POMGNT1) | ||
| ENST00000688596.1:n.593-7C>A (POMGNT1) | ||
| ENST00000688608.1:c.421-7C>A (POMGNT1) | ENSP00000508890.1:n.421-7C>A | |
| ENST00000688919.1:n.1227-7C>A (POMGNT1) | ||
| ENST00000689031.1:n.593-7C>A (POMGNT1) | ||
| ENST00000689717.1:n.593-7C>A (POMGNT1) | ||
| ENST00000689756.1:c.*53-7C>A (POMGNT1) | ENSP00000509023.1:n.*53-7C>A | |
| ENST00000690377.1:n.593-7C>A (POMGNT1) | ||
| ENST00000690678.1:c.421-7C>A (POMGNT1) | ENSP00000508703.1:n.421-7C>A | |
| ENST00000691209.1:c.421-7C>A (POMGNT1) | ENSP00000510112.1:n.421-7C>A | |
| ENST00000691243.1:c.421-7C>A (POMGNT1) | ENSP00000510654.1:n.421-7C>A | |
| ENST00000692169.1:n.593-7C>A (POMGNT1) | ||
| ENST00000692202.1:n.589-7C>A (POMGNT1) | ||
| ENST00000692322.1:c.*273-7C>A (POMGNT1) | ENSP00000509017.1:n.*273-7C>A | |
| ENST00000692369.1:c.421-7C>A (POMGNT1) | ENSP00000508453.1:n.421-7C>A | |
| ENST00000692599.1:n.593-7C>A (POMGNT1) | ||
| ENST00000692635.1:c.421-7C>A (POMGNT1) | ENSP00000508425.1:n.421-7C>A | |
| ENST00000693168.1:n.593-7C>A (POMGNT1) | ||
| ENST00000693218.1:c.421-7C>A (POMGNT1) | ENSP00000510577.1:n.421-7C>A | |
| ENST00000693223.1:n.1065-7C>A (POMGNT1) | ||
| ENST00000693365.1:n.1320-7C>A (POMGNT1) | ||
| ENST00000371984.8:c.421-7C>A (POMGNT1) MANE Select | ENSP00000361052.3:n.421-7C>A | |
| ENST00000371984.7:c.421-7C>A (POMGNT1) | ENSP00000361052.3:n.421-7C>A | |
| ENST00000371992.1:c.421-7C>A (POMGNT1) | ENSP00000361060.1:n.421-7C>A | |
| ENST00000396420.7:c.421-7C>A (POMGNT1) | ENSP00000379698.3:n.421-7C>A | |
| ENST00000489985.1:n.654-7C>A (POMGNT1) | ||
| ENST00000497439.5:n.545-7C>A (POMGNT1) | ||
| NM_001243766.1:c.421-7C>A (POMGNT1) | NP_001230695.1:n.421-7C>A | |
| NM_001290129.1:c.355-7C>A (POMGNT1) | NP_001277058.1:n.355-7C>A | |
| NM_001290130.1:c.-9-7C>A (POMGNT1) | NP_001277059.1:n.-9-7C>A | |
| NM_017739.3:c.421-7C>A (POMGNT1) | NP_060209.3:n.421-7C>A | |
| XM_005271010.1:c.421-7C>A (POMGNT1) | XP_005271067.1:n.421-7C>A | |
| XM_006710755.1:c.421-7C>A (POMGNT1) | XP_006710818.1:n.421-7C>A | |
| XM_006710756.1:c.421-7C>A (POMGNT1) | XP_006710819.1:n.421-7C>A | |
| XM_011540460.1:c.679-271G>T (TSPAN1) | XP_011538762.1:n.679-271G>T | |
| XM_011540461.1:c.634-271G>T (TSPAN1) | XP_011538763.1:n.634-271G>T | |
| XM_011541759.1:c.355-7C>A (POMGNT1) | XP_011540061.1:n.355-7C>A | |
| XM_011541760.1:c.355-7C>A (POMGNT1) | XP_011540062.1:n.355-7C>A | |
| XR_946706.1:n.580-7C>A (POMGNT1) | ||
| XM_011540460.3:c.679-271G>T (TSPAN1) | XP_011538762.1:n.679-271G>T | |
| XM_011541760.3:c.355-7C>A (POMGNT1) | XP_011540062.1:n.355-7C>A | |
| XM_017001690.1:c.421-7C>A (POMGNT1) | XP_016857179.1:n.421-7C>A | |
| NM_001243766.2:c.421-7C>A (POMGNT1) | NP_001230695.2:n.421-7C>A | |
| NM_001290129.2:c.355-7C>A (POMGNT1) | NP_001277058.2:n.355-7C>A | |
| NM_001290130.2:c.-9-7C>A (POMGNT1) | NP_001277059.2:n.-9-7C>A | |
| NM_017739.4:c.421-7C>A (POMGNT1) MANE Select | NP_060209.4:n.421-7C>A |