Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63941640_63941652delinsTGTTGAGGATGGG , CM000679.2:g.63941640_63941652delinsTGTTGAGGATGGG | GRCh38 |
| NC_000017.10:g.62019000_62019012delinsTGTTGAGGATGGG , CM000679.1:g.62019000_62019012delinsTGTTGAGGATGGG | GRCh37 |
| NC_000017.9:g.59372732_59372744delinsTGTTGAGGATGGG | NCBI36 |
| NG_011699.1:g.36267_36279delinsCCCATCCTCAACA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000435607.3:c.4630_4642delinsCCCATCCTCAACA MANE Select | ENSP00000396320.1:p.Pro1544= | |
| ENST00000578147.5:c.4630_4642delinsCCCATCCTCAACA | ENSP00000463963.1:p.Pro1544= | |
| NM_000334.4:c.4630_4642delinsCCCATCCTCAACA MANE Select | NP_000325.4:p.Pro1544= | |
| XM_005257566.3:c.4630_4642delinsCCCATCCTCAACA | XP_005257623.1:p.Pro1544= |