Linked Data
gnomAD v4:
20-33443595-CGCG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.33443597_33443599del , CM000682.2:g.33443597_33443599del | GRCh38 |
| NC_000020.10:g.32031403_32031405del , CM000682.1:g.32031403_32031405del | GRCh37 |
| NC_000020.9:g.31495064_31495066del | NCBI36 |
| NG_011622.1:g.5295_5297del , LRG_332:g.5295_5297del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000217381.3:c.23_25del MANE Select | ENSP00000217381.2:p.Pro8del | |
| ENST00000217381.2:c.23_25del | ENSP00000217381.2:p.Pro8del | |
| NM_003098.2:c.23_25del , LRG_332t1:c.23_25del | NP_003089.1:p.Pro8del | |
| XM_005260517.1:c.23_25del | XP_005260574.1:p.Pro8del | |
| XM_011529007.1:c.23_25del | XP_011527309.1:p.Pro8del | |
| XM_011529008.1:c.23_25del | XP_011527310.1:p.Pro8del | |
| XR_936612.1:n.256_258del | ||
| NM_003098.3:c.23_25del MANE Select | NP_003089.1:p.Pro8del |