Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94043505_94043506insACA , CM000663.2:g.94043505_94043506insACA | GRCh38 |
| NC_000001.10:g.94509061_94509062insACA , CM000663.1:g.94509061_94509062insACA | GRCh37 |
| NC_000001.9:g.94281649_94281650insACA | NCBI36 |
| NG_009073.1:g.82644_82645insTGT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.3051-31_3051-30insTGT MANE Select | ENSP00000359245.3:n.3051-31_3051-30insTGT | |
| ENST00000370225.3:c.3051-31_3051-30insTGT | ENSP00000359245.3:n.3051-31_3051-30insTGT | |
| ENST00000536513.5:c.-64-3417_-64-3416insTGT | ENSP00000439707.2:n.-64-3417_-64-3416insTGT | |
| NM_000350.2:c.3051-31_3051-30insTGT | NP_000341.2:n.3051-31_3051-30insTGT | |
| NM_000350.3:c.3051-31_3051-30insTGT MANE Select | NP_000341.2:n.3051-31_3051-30insTGT |