Linked Data
gnomAD v4:
1-15445495-GCT-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.15445496_15445497del , CM000663.2:g.15445496_15445497del | GRCh38 |
| NC_000001.10:g.15771991_15771992del , CM000663.1:g.15771991_15771992del | GRCh37 |
| NC_000001.9:g.15644578_15644579del | NCBI36 |
| NG_009253.1:g.12054_12055del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375949.5:c.640-101_640-100del MANE Select | ENSP00000365116.4:n.640-101_640-100del | |
| ENST00000375943.6:c.*94-101_*94-100del | ENSP00000365110.2:n.*94-101_*94-100del | |
| ENST00000375949.4:c.640-101_640-100del | ENSP00000365116.4:n.640-101_640-100del | |
| ENST00000483406.1:n.404-101_404-100del | ||
| NM_007272.2:c.640-101_640-100del | NP_009203.2:n.640-101_640-100del | |
| XM_011540550.1:c.494-101_494-100del | XP_011538852.1:n.494-101_494-100del | |
| NM_007272.3:c.640-101_640-100del MANE Select | NP_009203.2:n.640-101_640-100del |