Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133644181_133644182insATACGGC , CM000671.2:g.133644181_133644182insATACGGC | GRCh38 |
| NC_000009.11:g.136509303_136509304insATACGGC , CM000671.1:g.136509303_136509304insATACGGC | GRCh37 |
| NC_000009.10:g.135499124_135499125insATACGGC | NCBI36 |
| NG_008645.1:g.12819_12820insATACGGC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000393056.8:c.922-37_922-36insATACGGC MANE Select | ENSP00000376776.2:n.922-37_922-36insATACGGC | |
| ENST00000393056.6:c.922-37_922-36insATACGGC | ENSP00000376776.2:n.922-37_922-36insATACGGC | |
| NM_000787.3:c.922-37_922-36insATACGGC | NP_000778.3:n.922-37_922-36insATACGGC | |
| NM_000787.4:c.922-37_922-36insATACGGC MANE Select | NP_000778.3:n.922-37_922-36insATACGGC |