Linked Data
gnomAD v4:
10-94981161-GTTT-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94981164_94981166del , CM000672.2:g.94981164_94981166del | GRCh38 |
| NC_000010.10:g.96740921_96740923del , CM000672.1:g.96740921_96740923del | GRCh37 |
| NC_000010.9:g.96730911_96730913del | NCBI36 |
| NG_008385.1:g.47507_47509del | |
| NG_008385.2:g.48007_48009del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.962-19_962-17del MANE Select | ENSP00000260682.6:n.962-19_962-17del | |
| ENST00000643112.1:c.820-19_820-17del | ENSP00000496202.1:n.820-19_820-17del | |
| ENST00000260682.6:c.962-19_962-17del | ENSP00000260682.6:n.962-19_962-17del | |
| NM_000771.3:c.962-19_962-17del | NP_000762.2:n.962-19_962-17del | |
| NM_000771.4:c.962-19_962-17del MANE Select | NP_000762.2:n.962-19_962-17del |