Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52492670_52492673delinsCTTG , CM000674.2:g.52492670_52492673delinsCTTG | GRCh38 |
| NC_000012.11:g.52886454_52886457delinsCTTG , CM000674.1:g.52886454_52886457delinsCTTG | GRCh37 |
| NC_000012.10:g.51172721_51172724delinsCTTG | NCBI36 |
| NG_008298.1:g.5725_5728delinsCAAG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330722.7:c.516_519delinsCAAG MANE Select | ENSP00000369317.3:p.Asn172= | |
| ENST00000330722.6:c.516_519delinsCAAG | ENSP00000369317.3:p.Asn172= | |
| ENST00000549898.5:n.37_40delinsCAAG | ||
| NM_005554.3:c.516_519delinsCAAG | NP_005545.1:p.Asn172= | |
| NM_005554.4:c.516_519delinsCAAG MANE Select | NP_005545.1:p.Asn172= |