Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6714098_6714101delinsCGTT , CM000681.2:g.6714098_6714101delinsCGTT | GRCh38 |
| NC_000019.9:g.6714109_6714112delinsCGTT , CM000681.1:g.6714109_6714112delinsCGTT | GRCh37 |
| NC_000019.8:g.6665109_6665112delinsCGTT | NCBI36 |
| NG_009557.1:g.11551_11554delinsAACG , LRG_27:g.11551_11554delinsAACG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.560-19_560-16delinsAACG | ENSP00000512083.1:n.560-19_560-16delinsAACG | |
| ENST00000245907.11:c.683-19_683-16delinsAACG MANE Select | ENSP00000245907.4:n.683-19_683-16delinsAACG | |
| ENST00000245907.10:c.683-19_683-16delinsAACG | ENSP00000245907.4:n.683-19_683-16delinsAACG | |
| ENST00000595577.1:n.187-19_187-16delinsAACG | ||
| NM_000064.3:c.683-19_683-16delinsAACG | NP_000055.2:n.683-19_683-16delinsAACG | |
| NM_000064.4:c.683-19_683-16delinsAACG MANE Select | NP_000055.2:n.683-19_683-16delinsAACG |