Linked Data
gnomAD v4:
10-94780745-A-AAT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94780746_94780747insTA , CM000672.2:g.94780746_94780747insTA | GRCh38 |
| NC_000010.10:g.96540503_96540504insTA , CM000672.1:g.96540503_96540504insTA | GRCh37 |
| NC_000010.9:g.96530493_96530494insTA | NCBI36 |
| NG_008384.2:g.23041_23042insTA | |
| NG_008384.3:g.23066_23067insTA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.642+87_642+88insTA MANE Select | ENSP00000360372.3:n.642+87_642+88insTA | |
| ENST00000645461.1:n.1695+87_1695+88insTA | ||
| ENST00000371321.7:c.642+87_642+88insTA | ENSP00000360372.3:n.642+87_642+88insTA | |
| ENST00000464755.1:c.1405+87_1405+88insTA | ENSP00000483243.1:n.1405+87_1405+88insTA | |
| NM_000769.2:c.642+87_642+88insTA | NP_000760.1:n.642+87_642+88insTA | |
| NM_000769.4:c.642+87_642+88insTA MANE Select | NP_000760.1:n.642+87_642+88insTA |