Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1414421_1414426delinsCGGAGA , CM000667.2:g.1414421_1414426delinsCGGAGA | GRCh38 |
| NC_000005.9:g.1414536_1414541delinsCGGAGA , CM000667.1:g.1414536_1414541delinsCGGAGA | GRCh37 |
| NC_000005.8:g.1467536_1467541delinsCGGAGA | NCBI36 |
| NG_015885.1:g.36003_36008delinsTCTCCG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270349.12:c.1156+265_1156+270delinsTCTCCG MANE Select | ENSP00000270349.9:n.1156+265_1156+270delinsTCTCCG | |
| ENST00000270349.11:c.1156+265_1156+270delinsTCTCCG | ENSP00000270349.9:n.1156+265_1156+270delinsTCTCCG | |
| NM_001044.4:c.1156+265_1156+270delinsTCTCCG | NP_001035.1:n.1156+265_1156+270delinsTCTCCG | |
| NM_001044.5:c.1156+265_1156+270delinsTCTCCG MANE Select | NP_001035.1:n.1156+265_1156+270delinsTCTCCG |