Linked Data
gnomAD v2:
16-56936425-A-AGGGGGG
gnomAD v3:
16-56902513-A-AGGGGGG
gnomAD v4:
16-56902513-A-AGGGGGG
MyVariant Identifiers:
chr16:g.56936425_56936426insGGGGGG (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.56902514_56902515insGGGGGG , CM000678.2:g.56902514_56902515insGGGGGG | GRCh38 |
| NC_000016.9:g.56936426_56936427insGGGGGG , CM000678.1:g.56936426_56936427insGGGGGG | GRCh37 |
| NC_000016.8:g.55493927_55493928insGGGGGG | NCBI36 |
| NG_009386.1:g.42308_42309insGGGGGG | |
| NG_009386.2:g.42308_42309insGGGGGG |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000563236.6:c.2856+6_2856+7insGGGGGG MANE Select | ENSP00000456149.2:n.2856+6_2856+7insGGGGG... | |
| ENST00000262502.5:c.2853+6_2853+7insGGGGGG | ENSP00000262502.5:n.2853+6_2853+7insGGGGG... | |
| ENST00000438926.6:c.2883+6_2883+7insGGGGGG | ENSP00000402152.2:n.2883+6_2883+7insGGGGG... | |
| ENST00000563236.5:c.2856+6_2856+7insGGGGGG | ENSP00000456149.1:n.2856+6_2856+7insGGGGG... | |
| ENST00000566786.5:c.2880+6_2880+7insGGGGGG | ENSP00000457552.1:n.2880+6_2880+7insGGGGG... | |
| ENST00000569002.1:n.287+6_287+7insGGGGGG | ||
| NM_000339.2:c.2883+6_2883+7insGGGGGG | NP_000330.2:n.2883+6_2883+7insGGGGGG | |
| NM_001126107.1:c.2880+6_2880+7insGGGGGG | NP_001119579.1:n.2880+6_2880+7insGGGGGG | |
| NM_001126108.1:c.2856+6_2856+7insGGGGGG | NP_001119580.1:n.2856+6_2856+7insGGGGGG | |
| XM_005256119.1:c.2853+6_2853+7insGGGGGG | XP_005256176.1:n.2853+6_2853+7insGGGGGG | |
| XM_005256119.2:c.2853+6_2853+7insGGGGGG | XP_005256176.1:n.2853+6_2853+7insGGGGGG | |
| NM_000339.3:c.2883+6_2883+7insGGGGGG | NP_000330.3:n.2883+6_2883+7insGGGGGG | |
| NM_001126107.2:c.2880+6_2880+7insGGGGGG | NP_001119579.2:n.2880+6_2880+7insGGGGGG | |
| NM_001126108.2:c.2856+6_2856+7insGGGGGG MANE Select | NP_001119580.2:n.2856+6_2856+7insGGGGGG |