Linked Data
MyVariant Identifiers:
chr15:g.73614903_73614904insG (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73322562_73322563insG , CM000677.2:g.73322562_73322563insG | GRCh38 |
| NC_000015.9:g.73614903_73614904insG , CM000677.1:g.73614903_73614904insG | GRCh37 |
| NC_000015.8:g.71401956_71401957insG | NCBI36 |
| NG_009063.1:g.51702_51703insC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.3530_3531insC MANE Select | ENSP00000261917.3:p.Pro1178AlafsTer16 | |
| ENST00000261917.3:c.3530_3531insC | ENSP00000261917.3:p.Pro1178AlafsTer16 | |
| NM_005477.2:c.3530_3531insC | NP_005468.1:p.Pro1178AlafsTer16 | |
| XM_011521148.1:c.2312_2313insC | XP_011519450.1:p.Pro772AlafsTer16 | |
| XM_011521148.2:c.2312_2313insC | XP_011519450.1:p.Pro772AlafsTer16 | |
| NM_005477.3:c.3530_3531insC MANE Select | NP_005468.1:p.Pro1178AlafsTer16 |