Linked Data
gnomAD v4:
10-94763004-TG-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94763005del , CM000672.2:g.94763005del | GRCh38 |
| NC_000010.10:g.96522762del , CM000672.1:g.96522762del | GRCh37 |
| NC_000010.9:g.96512752del | NCBI36 |
| NG_008384.2:g.5300del | |
| NG_008384.3:g.5325del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.168+132del MANE Select | ENSP00000360372.3:n.168+132del | |
| ENST00000371321.7:c.168+132del | ENSP00000360372.3:n.168+132del | |
| ENST00000464755.1:c.932-12053del | ENSP00000483243.1:n.932-12053del | |
| ENST00000480405.2:c.168+132del | ENSP00000483847.1:n.168+132del | |
| NM_000769.2:c.168+132del | NP_000760.1:n.168+132del | |
| NM_000769.4:c.168+132del MANE Select | NP_000760.1:n.168+132del |