HGVS | Genome Assembly |
---|---|
NC_000016.10:g.173143_173144insGAA , CM000678.2:g.173143_173144insGAA | GRCh38 |
NC_000016.9:g.223142_223143insGAA , CM000678.1:g.223142_223143insGAA | GRCh37 |
NC_000016.8:g.163142_163143insGAA | NCBI36 |
NG_000006.1:g.34006_34007insGAA | |
NG_059186.1:g.1493_1494insGAA | |
NG_059271.1:g.5297_5298insGAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251595.11:c.114_115insGAA MANE Select | ENSP00000251595.6:p.Pro38_Thr39insGlu | |
ENST00000251595.10:c.114_115insGAA | ENSP00000251595.6:p.Pro38_Thr39insGlu | |
ENST00000397806.1:c.18_19insGAA | ENSP00000380908.1:p.Pro6_Thr7insGlu | |
ENST00000482565.1:n.250_251insGAA | ||
ENST00000484216.1:n.83_84insGAA | ||
NM_000517.4:c.114_115insGAA | NP_000508.1:p.Pro38_Thr39insGlu | |
NM_000517.6:c.114_115insGAA MANE Select | NP_000508.1:p.Pro38_Thr39insGlu |