Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226949delinsGTG , CM000673.2:g.5226949delinsGTG | GRCh38 |
| NC_000011.9:g.5248179delinsGTG , CM000673.1:g.5248179delinsGTG | GRCh37 |
| NC_000011.8:g.5204755delinsGTG | NCBI36 |
| NG_000007.3:g.70667delinsCAC | |
| NG_059281.1:g.5123delinsCAC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.73delinsCAC | ENSP00000494175.1:p.Gly25HisfsTer? | |
| ENST00000335295.4:c.73delinsCAC MANE Select | ENSP00000333994.3:p.Gly25HisfsTer? | |
| ENST00000380315.2:c.73delinsCAC | ENSP00000369671.2:p.Gly25HisfsTer? | |
| ENST00000485743.1:n.124delinsCAC | ||
| ENST00000633227.1:c.73delinsCAC | ENSP00000488004.1:p.Gly25HisfsTer15 | |
| NM_000518.4:c.73delinsCAC | NP_000509.1:p.Gly25HisfsTer? | |
| NM_000518.5:c.73delinsCAC MANE Select | NP_000509.1:p.Gly25HisfsTer? |