Linked Data
gnomAD v4:
20-33443544-TCGC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.33443550_33443552del , CM000682.2:g.33443550_33443552del | GRCh38 |
| NC_000020.10:g.32031356_32031358del , CM000682.1:g.32031356_32031358del | GRCh37 |
| NC_000020.9:g.31495017_31495019del | NCBI36 |
| NG_011622.1:g.5346_5348del , LRG_332:g.5346_5348del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000217381.3:c.74_76del MANE Select | ENSP00000217381.2:p.Gly25del | |
| ENST00000217381.2:c.74_76del | ENSP00000217381.2:p.Gly25del | |
| NM_003098.2:c.74_76del , LRG_332t1:c.74_76del | NP_003089.1:p.Gly25del | |
| XM_005260517.1:c.74_76del | XP_005260574.1:p.Gly25del | |
| XM_011529007.1:c.74_76del | XP_011527309.1:p.Gly25del | |
| XM_011529008.1:c.74_76del | XP_011527310.1:p.Gly25del | |
| XR_936612.1:n.307_309del | ||
| NM_003098.3:c.74_76del MANE Select | NP_003089.1:p.Gly25del |