Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226948delinsGTG , CM000673.2:g.5226948delinsGTG | GRCh38 |
| NC_000011.9:g.5248178delinsGTG , CM000673.1:g.5248178delinsGTG | GRCh37 |
| NC_000011.8:g.5204754delinsGTG | NCBI36 |
| NG_000007.3:g.70668delinsCAC | |
| NG_059281.1:g.5124delinsCAC |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000518.5:c.74delinsCAC MANE Select | NP_000509.1:p.Gly25AlafsTer? |
| ENST00000335295.4:c.74delinsCAC MANE Select | ENSP00000333994.3:p.Gly25AlafsTer? |
| NM_000518.4:c.74delinsCAC | NP_000509.1:p.Gly25AlafsTer? |
| ENST00000380315.2:c.74delinsCAC | ENSP00000369671.2:p.Gly25AlafsTer? |
| ENST00000485743.1:n.125delinsCAC | |
| ENST00000633227.1:c.74delinsCAC | ENSP00000488004.1:p.Gly25AlafsTer15 |
| ENST00000647020.1:c.74delinsCAC | ENSP00000494175.1:p.Gly25AlafsTer? |