Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226983_5226984insCCACCCCG , CM000673.2:g.5226983_5226984insCCACCCCG | GRCh38 |
| NC_000011.9:g.5248213_5248214insCCACCCCG , CM000673.1:g.5248213_5248214insCCACCCCG | GRCh37 |
| NC_000011.8:g.5204789_5204790insCCACCCCG | NCBI36 |
| NG_000007.3:g.70632_70633insCGGGGTGG | |
| NG_059281.1:g.5088_5089insCGGGGTGG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.38_39insCGGGGTGG | ENSP00000494175.1:p.Ala14GlyfsTer9 | |
| ENST00000335295.4:c.38_39insCGGGGTGG MANE Select | ENSP00000333994.3:p.Ala14GlyfsTer9 | |
| ENST00000380315.2:c.38_39insCGGGGTGG | ENSP00000369671.2:p.Ala14GlyfsTer9 | |
| ENST00000485743.1:n.89_90insCGGGGTGG | ||
| ENST00000633227.1:c.38_39insCGGGGTGG | ENSP00000488004.1:p.Ala14GlyfsTer9 | |
| NM_000518.4:c.38_39insCGGGGTGG | NP_000509.1:p.Ala14GlyfsTer9 | |
| NM_000518.5:c.38_39insCGGGGTGG MANE Select | NP_000509.1:p.Ala14GlyfsTer9 |