Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94047169_94047170insAC , CM000663.2:g.94047169_94047170insAC | GRCh38 |
| NC_000001.10:g.94512725_94512726insAC , CM000663.1:g.94512725_94512726insAC | GRCh37 |
| NC_000001.9:g.94285313_94285314insAC | NCBI36 |
| NG_009073.1:g.78980_78981insGT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.2744-77_2744-76insGT MANE Select | ENSP00000359245.3:n.2744-77_2744-76insGT | |
| ENST00000649773.1:c.2522-77_2522-76insGT | ENSP00000496882.1:n.2522-77_2522-76insGT | |
| ENST00000370225.3:c.2744-77_2744-76insGT | ENSP00000359245.3:n.2744-77_2744-76insGT | |
| ENST00000536513.5:c.-64-7081_-64-7080insGT | ENSP00000439707.2:n.-64-7081_-64-7080insGT | |
| NM_000350.2:c.2744-77_2744-76insGT | NP_000341.2:n.2744-77_2744-76insGT | |
| NM_000350.3:c.2744-77_2744-76insGT MANE Select | NP_000341.2:n.2744-77_2744-76insGT |