Linked Data
MyVariant Identifiers:
chr10:g.82034862_82034864del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.80275106_80275108del , CM000672.2:g.80275106_80275108del | GRCh38 |
| NC_000010.10:g.82034862_82034864del , CM000672.1:g.82034862_82034864del | GRCh37 |
| NC_000010.9:g.82024842_82024844del | NCBI36 |
| NG_008083.1:g.19571_19573del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372213.8:c.860_862del MANE Select | ENSP00000361287.3:p.Tyr287_Thr288delinsSer | |
| ENST00000372213.7:c.860_862del | ENSP00000361287.3:p.Tyr287_Thr288delinsSer | |
| ENST00000480845.1:n.92_94del | ||
| ENST00000485270.5:n.372_374del | ||
| NM_000429.2:c.860_862del | NP_000420.1:p.Tyr287_Thr288delinsSer | |
| XM_005269842.3:c.860_862del | XP_005269899.1:p.Tyr287_Thr288delinsSer | |
| XM_005269843.3:c.737_739del | XP_005269900.1:p.Tyr246_Thr247delinsSer | |
| NM_000429.3:c.860_862del MANE Select | NP_000420.1:p.Tyr287_Thr288delinsSer |