Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94418440_94418441insACG , CM000663.2:g.94418440_94418441insACG | GRCh38 |
| NC_000001.10:g.94883996_94883997insACG , CM000663.1:g.94883996_94883997insACG | GRCh37 |
| NC_000001.9:g.94656584_94656585insACG | NCBI36 |
| NG_008865.1:g.5064_5065insACG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370214.9:c.-39_-38insACG MANE Select | ENSP00000359233.4:n.-39_-38insACG | |
| NM_001122674.1:c.-39_-38insACG | NP_001116146.1:n.-39_-38insACG | |
| NM_002858.3:c.-39_-38insACG | NP_002849.1:n.-39_-38insACG | |
| XM_006710802.2:c.-39_-38insACG | XP_006710865.2:n.-39_-38insACG | |
| NM_002858.4:c.-39_-38insACG MANE Select | NP_002849.1:n.-39_-38insACG | |
| NM_001122674.2:c.-39_-38insACG | NP_001116146.1:n.-39_-38insACG |