Linked Data
gnomAD v4:
10-94941700-TA-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94941702del , CM000672.2:g.94941702del | GRCh38 |
| NC_000010.10:g.96701459del , CM000672.1:g.96701459del | GRCh37 |
| NC_000010.9:g.96691449del | NCBI36 |
| NG_008385.1:g.8045del | |
| NG_008385.2:g.8545del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.169-156del MANE Select | ENSP00000260682.6:n.169-156del | |
| ENST00000643112.1:c.169-156del | ENSP00000496202.1:n.169-156del | |
| ENST00000645207.1:n.166del | ||
| ENST00000260682.6:c.169-156del | ENSP00000260682.6:n.169-156del | |
| ENST00000461906.1:n.194-156del | ||
| NM_000771.3:c.169-156del | NP_000762.2:n.169-156del | |
| NM_000771.4:c.169-156del MANE Select | NP_000762.2:n.169-156del |