Linked Data
MyVariant Identifiers:
chr10:g.96708876_96708877insG (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94949119_94949120insG , CM000672.2:g.94949119_94949120insG | GRCh38 |
| NC_000010.10:g.96708876_96708877insG , CM000672.1:g.96708876_96708877insG | GRCh37 |
| NC_000010.9:g.96698866_96698867insG | NCBI36 |
| NG_008385.1:g.15462_15463insG | |
| NG_008385.2:g.15962_15963insG |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260682.8:c.654_655insG MANE Select | ENSP00000260682.6:p.Phe219ValfsTer6 | |
| ENST00000643112.1:c.654_655insG | ENSP00000496202.1:p.Phe219ValfsTer6 | |
| ENST00000260682.6:c.654_655insG | ENSP00000260682.6:p.Phe219ValfsTer6 | |
| ENST00000473496.1:n.425_426insG | ||
| NM_000771.3:c.654_655insG | NP_000762.2:p.Phe219ValfsTer6 | |
| NM_000771.4:c.654_655insG MANE Select | NP_000762.2:p.Phe219ValfsTer6 |