Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94030592_94030593insAGA , CM000663.2:g.94030592_94030593insAGA | GRCh38 |
| NC_000001.10:g.94496148_94496149insAGA , CM000663.1:g.94496148_94496149insAGA | GRCh37 |
| NC_000001.9:g.94268736_94268737insAGA | NCBI36 |
| NG_009073.1:g.95557_95558insTCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.4254-67_4254-66insTCT MANE Select | ENSP00000359245.3:n.4254-67_4254-66insTCT | |
| ENST00000370225.3:c.4254-67_4254-66insTCT | ENSP00000359245.3:n.4254-67_4254-66insTCT | |
| ENST00000536513.5:c.630-67_630-66insTCT | ENSP00000439707.2:n.630-67_630-66insTCT | |
| NM_000350.2:c.4254-67_4254-66insTCT | NP_000341.2:n.4254-67_4254-66insTCT | |
| NM_000350.3:c.4254-67_4254-66insTCT MANE Select | NP_000341.2:n.4254-67_4254-66insTCT |