Linked Data
gnomAD v4:
10-94775562-A-AG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94775562_94775563insG , CM000672.2:g.94775562_94775563insG | GRCh38 |
| NC_000010.10:g.96535319_96535320insG , CM000672.1:g.96535319_96535320insG | GRCh37 |
| NC_000010.9:g.96525309_96525310insG | NCBI36 |
| NG_008384.2:g.17857_17858insG | |
| NG_008384.3:g.17882_17883insG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.481+23_481+24insG MANE Select | ENSP00000360372.3:n.481+23_481+24insG | |
| ENST00000645461.1:n.1534+23_1534+24insG | ||
| ENST00000371321.7:c.481+23_481+24insG | ENSP00000360372.3:n.481+23_481+24insG | |
| ENST00000464755.1:c.1244+23_1244+24insG | ENSP00000483243.1:n.1244+23_1244+24insG | |
| ENST00000480405.2:c.*15_*16insG | ENSP00000483847.1:n.*15_*16insG | |
| NM_000769.2:c.481+23_481+24insG | NP_000760.1:n.481+23_481+24insG | |
| NM_000769.4:c.481+23_481+24insG MANE Select | NP_000760.1:n.481+23_481+24insG |