Linked Data
gnomAD v4:
10-94781785-ATGCTT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94781787_94781791del , CM000672.2:g.94781787_94781791del | GRCh38 |
| NC_000010.10:g.96541544_96541548del , CM000672.1:g.96541544_96541548del | GRCh37 |
| NC_000010.9:g.96531534_96531538del | NCBI36 |
| NG_008384.2:g.24082_24086del | |
| NG_008384.3:g.24107_24111del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.643-34_643-30del MANE Select | ENSP00000360372.3:n.643-34_643-30del | |
| ENST00000645461.1:n.1696-34_1696-30del | ||
| ENST00000371321.7:c.643-34_643-30del | ENSP00000360372.3:n.643-34_643-30del | |
| ENST00000464755.1:c.1406-34_1406-30del | ENSP00000483243.1:n.1406-34_1406-30del | |
| NM_000769.2:c.643-34_643-30del | NP_000760.1:n.643-34_643-30del | |
| NM_000769.4:c.643-34_643-30del MANE Select | NP_000760.1:n.643-34_643-30del |