Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.15999701dup , CM000679.2:g.15999701dup | GRCh38 |
| NC_000017.10:g.15903015dup , CM000679.1:g.15903015dup | GRCh37 |
| NC_000017.9:g.15843740dup | NCBI36 |
| NG_029806.1:g.5322dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000399277.6:c.-106dup (ZSWIM7) MANE Select | ENSP00000382218.1:n.-106dup | |
| ENST00000261647.9:c.-148dup (TTC19) | ENSP00000261647.5:n.-148dup | |
| ENST00000491631.5:c.-106dup (ZSWIM7) | ENSP00000462598.1:n.-106dup | |
| ENST00000497719.5:n.14dup (ZSWIM7) | ||
| NM_001271420.1:c.-606dup (TTC19) | NP_001258349.1:n.-606dup | |
| NM_017775.3:c.-148dup (TTC19) | NP_060245.3:n.-148dup | |
| NM_001042697.2:c.-106dup (ZSWIM7) MANE Select | NP_001036162.1:n.-106dup | |
| NM_001042698.2:c.-106dup (ZSWIM7) | NP_001036163.1:n.-106dup |