Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.28767413_28767424dup , CM000676.2:g.28767413_28767424dup | GRCh38 |
| NC_000014.8:g.29236619_29236630dup , CM000676.1:g.29236619_29236630dup | GRCh37 |
| NC_000014.7:g.28306370_28306381dup | NCBI36 |
| NG_009367.1:g.5333_5344dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706482.1:c.134_145dup | ENSP00000516406.1:p.His48_His49insProGlnHisHis | |
| ENST00000313071.7:c.134_145dup MANE Select | ENSP00000339004.3:p.His48_His49insProGlnHisHis | |
| ENST00000313071.6:c.134_145dup | ENSP00000339004.3:p.His48_His49insProGlnHisHis | |
| NM_005249.4:c.134_145dup | NP_005240.3:p.His48_His49insProGlnHisHis | |
| NM_005249.5:c.134_145dup MANE Select | NP_005240.3:p.His48_His49insProGlnHisHis |