Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29070995_29070999delinsTGGGG , CM000664.2:g.29070995_29070999delinsTGGGG | GRCh38 |
| NC_000002.11:g.29293861_29293865delinsTGGGG , CM000664.1:g.29293861_29293865delinsTGGGG | GRCh37 |
| NC_000002.10:g.29147365_29147369delinsTGGGG | NCBI36 |
| NG_021427.1:g.8263_8267delinsCCCCA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331664.6:c.3263_3267delinsCCCCA MANE Select | ENSP00000332809.4:p.Ser1088= | |
| ENST00000331664.5:c.3263_3267delinsCCCCA | ENSP00000332809.4:p.Ser1088= | |
| NM_001029883.2:c.3263_3267delinsCCCCA | NP_001025054.1:p.Ser1088= | |
| XM_011532826.1:c.3263_3267delinsCCCCA | XP_011531128.1:p.Ser1088= | |
| XR_939901.1:n.185+1828_185+1832delinsTGGGG | ||
| XR_939902.1:n.173+1840_173+1844delinsTGGGG | ||
| NM_001029883.3:c.3263_3267delinsCCCCA MANE Select | NP_001025054.1:p.Ser1088= |