Linked Data
MyVariant Identifiers:
chr10:g.82034866_82034867insGGA (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.80275110_80275111insGGA , CM000672.2:g.80275110_80275111insGGA | GRCh38 |
| NC_000010.10:g.82034866_82034867insGGA , CM000672.1:g.82034866_82034867insGGA | GRCh37 |
| NC_000010.9:g.82024846_82024847insGGA | NCBI36 |
| NG_008083.1:g.19568_19569insTCC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372213.8:c.857_858insTCC MANE Select | ENSP00000361287.3:p.Asp286_Tyr287insPro | |
| ENST00000372213.7:c.857_858insTCC | ENSP00000361287.3:p.Asp286_Tyr287insPro | |
| ENST00000480845.1:n.89_90insTCC | ||
| ENST00000485270.5:n.369_370insTCC | ||
| NM_000429.2:c.857_858insTCC | NP_000420.1:p.Asp286_Tyr287insPro | |
| XM_005269842.3:c.857_858insTCC | XP_005269899.1:p.Asp286_Tyr287insPro | |
| XM_005269843.3:c.734_735insTCC | XP_005269900.1:p.Asp245_Tyr246insPro | |
| NM_000429.3:c.857_858insTCC MANE Select | NP_000420.1:p.Asp286_Tyr287insPro |