Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114714015_114714016insCGGC , CM000663.2:g.114714015_114714016insCGGC | GRCh38 |
| NC_000001.10:g.115256636_115256637insCGGC , CM000663.1:g.115256636_115256637insCGGC | GRCh37 |
| NC_000001.9:g.115058159_115058160insCGGC | NCBI36 |
| NG_007572.1:g.7879_7880insGCCG , LRG_92:g.7879_7880insGCCG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369535.5:c.112-38_112-37insGCCG MANE Select | ENSP00000358548.4:n.112-38_112-37insGCCG | |
| ENST00000369535.4:c.112-38_112-37insGCCG | ENSP00000358548.4:n.112-38_112-37insGCCG | |
| NM_002524.4:c.112-38_112-37insGCCG | NP_002515.1:n.112-38_112-37insGCCG | |
| NM_002524.5:c.112-38_112-37insGCCG MANE Select | NP_002515.1:n.112-38_112-37insGCCG |