Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25004798_25004839delinsCCGGGTCGGCCAGGGCGCCCGATGCCACTGCGCCCTCCACGG , CM000685.2:g.25004798_25004839delinsCCGGGTCGGCCAGGGCGCCCGATGCCACTGCGCCCTCCACGG | GRCh38 |
| NC_000023.10:g.25022915_25022956delinsCCGGGTCGGCCAGGGCGCCCGATGCCACTGCGCCCTCCACGG , CM000685.1:g.25022915_25022956delinsCCGGGTCGGCCAGGGCGCCCGATGCCACTGCGCCCTCCACGG | GRCh37 |
| NC_000023.9:g.24932836_24932877delinsCCGGGTCGGCCAGGGCGCCCGATGCCACTGCGCCCTCCACGG | NCBI36 |
| NG_008281.1:g.16110_16151delinsCCGTGGAGGGCGCAGTGGCATCGGGCGCCCTGGCCGACCCGG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379044.5:c.1520_1561delinsCCGTGGAGGGCGCAGTGGCATCGGGCGCCCTGGCCGACCCGG MANE Select | ENSP00000368332.4:p.Ala507= | |
| ENST00000379044.4:c.1520_1561delinsCCGTGGAGGGCGCAGTGGCATCGGGCGCCCTGGCCGACCCGG | ENSP00000368332.4:p.Ala507= | |
| NM_139058.2:c.1520_1561delinsCCGTGGAGGGCGCAGTGGCATCGGGCGCCCTGGCCGACCCGG | NP_620689.1:p.Ala507= | |
| NM_139058.3:c.1520_1561delinsCCGTGGAGGGCGCAGTGGCATCGGGCGCCCTGGCCGACCCGG MANE Select | NP_620689.1:p.Ala507= |