Linked Data
MyVariant Identifiers:
chr17:g.40688301dup (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42536283dup , CM000679.2:g.42536283dup | GRCh38 |
| NC_000017.10:g.40688301dup , CM000679.1:g.40688301dup | GRCh37 |
| NC_000017.9:g.37941827dup | NCBI36 |
| NG_011552.1:g.5351dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.11dup MANE Select | ENSP00000225927.1:p.Ala5GlyfsTer? | |
| ENST00000225927.6:c.11dup | ENSP00000225927.1:p.Ala5GlyfsTer? | |
| NM_000263.3:c.11dup | NP_000254.2:p.Ala5GlyfsTer? | |
| XM_024450771.1:c.11dup | XP_024306539.1:p.Ala5GlyfsTer? | |
| NM_000263.4:c.11dup MANE Select | NP_000254.2:p.Ala5GlyfsTer? |