Linked Data
gnomAD v4:
5-10286406-G-GTGTTCC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.10286406_10286407insTGTTCC , CM000667.2:g.10286406_10286407insTGTTCC | GRCh38 |
| NC_000005.9:g.10286518_10286519insTGTTCC , CM000667.1:g.10286518_10286519insTGTTCC | GRCh37 |
| NC_000005.8:g.10339518_10339519insTGTTCC | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296658.4:c.413_414insGGAACA MANE Select | ENSP00000296658.3:p.Val138_His139insGluHis | |
| ENST00000296658.3:c.413_414insGGAACA | ENSP00000296658.3:p.Val138_His139insGluHis | |
| ENST00000506821.1:n.667_668insGGAACA | ||
| ENST00000510532.5:n.481_482insGGAACA | ||
| ENST00000511963.5:n.521_522insGGAACA | ||
| NM_138809.3:c.413_414insGGAACA | NP_620164.1:p.Val138_His139insGluHis | |
| NM_138809.4:c.413_414insGGAACA MANE Select | NP_620164.1:p.Val138_His139insGluHis |