Linked Data
gnomAD v4:
17-39665483-T-TA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39665483_39665484insA , CM000679.2:g.39665483_39665484insA | GRCh38 |
| NC_000017.10:g.37821736_37821737insA , CM000679.1:g.37821736_37821737insA | GRCh37 |
| NC_000017.9:g.35075262_35075263insA | NCBI36 |
| NG_008892.1:g.5138_5139insA , LRG_210:g.5138_5139insA | |
| NG_042278.1:g.2503_2504insA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309889.3:c.110+14_110+15insA MANE Select | ENSP00000312624.2:n.110+14_110+15insA | |
| ENST00000309889.2:c.110+14_110+15insA | ENSP00000312624.2:n.110+14_110+15insA | |
| ENST00000578283.1:c.110+14_110+15insA | ENSP00000462787.1:n.110+14_110+15insA | |
| NM_003673.3:c.110+14_110+15insA , LRG_210t1:c.110+14_110+15insA | NP_003664.1:n.110+14_110+15insA | |
| NM_003673.4:c.110+14_110+15insA MANE Select | NP_003664.1:n.110+14_110+15insA |