Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129529354_129529356delinsCTG , CM000665.2:g.129529354_129529356delinsCTG | GRCh38 |
| NC_000003.11:g.129248197_129248199delinsCTG , CM000665.1:g.129248197_129248199delinsCTG | GRCh37 |
| NC_000003.10:g.130730887_130730889delinsCTG | NCBI36 |
| NG_009115.1:g.5716_5718delinsCTG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296271.4:c.361+260_361+262delinsCTG MANE Select | ENSP00000296271.3:n.361+260_361+262delinsCTG | |
| ENST00000296271.3:c.361+260_361+262delinsCTG | ENSP00000296271.3:n.361+260_361+262delinsCTG | |
| NM_000539.3:c.361+260_361+262delinsCTG MANE Select | NP_000530.1:n.361+260_361+262delinsCTG |