Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.38071309dup , CM000664.2:g.38071309dup | GRCh38 |
| NC_000002.11:g.38298452dup , CM000664.1:g.38298452dup | GRCh37 |
| NC_000002.10:g.38151956dup | NCBI36 |
| NG_008386.2:g.9793dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000490576.2:c.1045dup | ENSP00000478839.2:p.Tyr349LeufsTer3 | |
| ENST00000610745.5:c.1045dup MANE Select | ENSP00000478561.1:p.Tyr349LeufsTer3 | |
| ENST00000492443.1:n.423dup | ||
| ENST00000494864.1:c.-69dup | ENSP00000479876.1:n.-69dup | |
| ENST00000610745.4:c.1045dup | ENSP00000478561.1:p.Tyr349LeufsTer3 | |
| ENST00000613082.1:n.440dup | ||
| ENST00000614273.1:c.1045dup | ENSP00000483678.1:p.Tyr349LeufsTer3 | |
| NM_000104.3:c.1045dup | NP_000095.2:p.Tyr349LeufsTer3 | |
| NM_000104.4:c.1045dup MANE Select | NP_000095.2:p.Tyr349LeufsTer3 |