Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.28767516_28767518dup , CM000676.2:g.28767516_28767518dup | GRCh38 |
| NC_000014.8:g.29236722_29236724dup , CM000676.1:g.29236722_29236724dup | GRCh37 |
| NC_000014.7:g.28306473_28306475dup | NCBI36 |
| NG_009367.1:g.5436_5438dup |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005249.5:c.237_239dup MANE Select | NP_005240.3:p.Pro80_Ala81insPro |
| ENST00000313071.7:c.237_239dup MANE Select | ENSP00000339004.3:p.Pro80_Ala81insPro |
| NM_005249.4:c.237_239dup | NP_005240.3:p.Pro80_Ala81insPro |
| ENST00000313071.6:c.237_239dup | ENSP00000339004.3:p.Pro80_Ala81insPro |
| ENST00000706482.1:c.237_239dup | ENSP00000516406.1:p.Pro80_Ala81insPro |