Linked Data
gnomAD v4:
1-15440449-AG-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.15440452del , CM000663.2:g.15440452del | GRCh38 |
| NC_000001.10:g.15766948del , CM000663.1:g.15766948del | GRCh37 |
| NC_000001.9:g.15639535del | NCBI36 |
| NG_009253.1:g.7011del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375949.5:c.133-41del MANE Select | ENSP00000365116.4:n.133-41del | |
| ENST00000375943.6:c.40+1948del | ENSP00000365110.2:n.40+1948del | |
| ENST00000375949.4:c.133-41del | ENSP00000365116.4:n.133-41del | |
| ENST00000476813.5:n.52+1948del | ||
| ENST00000483406.1:n.43-41del | ||
| NM_007272.2:c.133-41del | NP_009203.2:n.133-41del | |
| XM_011540550.1:c.133-41del | XP_011538852.1:n.133-41del | |
| NM_007272.3:c.133-41del MANE Select | NP_009203.2:n.133-41del |