Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31269077_31269078insC , CM000668.2:g.31269077_31269078insC | GRCh38 |
| NC_000006.11:g.31236854_31236855insC , CM000668.1:g.31236854_31236855insC | GRCh37 |
| NC_000006.10:g.31344833_31344834insC | NCBI36 |
| NG_029422.2:g.8054_8055insG |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000376228.10:c.*91_*92insG MANE Select | ENSP00000365402.5:n.*91_*92insG | |
| ENST00000376228.9:c.*91_*92insG | ENSP00000365402.5:n.*91_*92insG | |
| ENST00000376237.8:c.*779_*780insG | ENSP00000365412.4:n.*779_*780insG | |
| ENST00000383329.7:c.*91_*92insG | ENSP00000372819.3:n.*91_*92insG | |
| ENST00000466892.5:n.425_426insG | ||
| ENST00000470363.5:n.950_951insG | ||
| ENST00000487245.5:n.1551_1552insG | ||
| NM_002117.5:c.*91_*92insG | NP_002108.4:n.*91_*92insG | |
| NM_002117.6:c.*91_*92insG MANE Select | NP_002108.4:n.*91_*92insG |