Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86739743_86739744delinsGA , CM000670.2:g.86739743_86739744delinsGA | GRCh38 |
| NC_000008.10:g.87751971_87751972delinsGA , CM000670.1:g.87751971_87751972delinsGA | GRCh37 |
| NC_000008.9:g.87821087_87821088delinsGA | NCBI36 |
| NG_016980.1:g.8932_8933delinsTC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.130-8_130-7delinsTC MANE Select | ENSP00000316605.5:n.130-8_130-7delinsTC | |
| ENST00000681746.1:c.130-8_130-7delinsTC | ENSP00000505959.1:n.130-8_130-7delinsTC | |
| ENST00000320005.5:c.130-8_130-7delinsTC | ENSP00000316605.5:n.130-8_130-7delinsTC | |
| ENST00000519777.1:n.112-8_112-7delinsTC | ||
| NM_019098.4:c.130-8_130-7delinsTC | NP_061971.3:n.130-8_130-7delinsTC | |
| NM_019098.5:c.130-8_130-7delinsTC MANE Select | NP_061971.3:n.130-8_130-7delinsTC |