Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.116172600_116172602delinsGAT , CM000685.2:g.116172600_116172602delinsGAT | GRCh38 |
| NC_000023.10:g.115303853_115303855delinsGAT , CM000685.1:g.115303853_115303855delinsGAT | GRCh37 |
| NC_000023.9:g.115217881_115217883delinsGAT | NCBI36 |
| NG_016326.1:g.6896_6898delinsGAT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371906.5:c.320_322delinsGAT MANE Select | ENSP00000360973.4:p.Arg107= | |
| ENST00000680409.1:n.788_790delinsGAT | ||
| ENST00000681852.1:c.320_322delinsGAT | ENSP00000505750.1:p.Arg107= | |
| ENST00000371906.4:c.320_322delinsGAT | ENSP00000360973.4:p.Arg107= | |
| NM_000686.4:c.320_322delinsGAT | NP_000677.2:p.Arg107= | |
| XM_011537533.1:c.320_322delinsGAT | XP_011535835.1:p.Arg107= | |
| NM_000686.5:c.320_322delinsGAT MANE Select | NP_000677.2:p.Arg107= | |
| NM_001385624.1:c.320_322delinsGAT | NP_001372553.1:p.Arg107= |