HGVS | Genome Assembly |
---|---|
NC_000017.11:g.70175395_70175396insAAAATAA , CM000679.2:g.70175395_70175396insAAAATAA | GRCh38 |
NC_000017.10:g.68171536_68171537insAAAATAA , CM000679.1:g.68171536_68171537insAAAATAA | GRCh37 |
NC_000017.9:g.65683131_65683132insAAAATAA | NCBI36 |
NG_008798.1:g.10861_10862insAAAATAA , LRG_328:g.10861_10862insAAAATAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000243457.4:c.356_357insAAAATAA MANE Select | ENSP00000243457.2:p.Ala121Ter | |
ENST00000243457.3:c.356_357insAAAATAA | ENSP00000243457.2:p.Ala121Ter | |
ENST00000535240.1:c.356_357insAAAATAA | ENSP00000441848.1:p.Ala121Ter | |
NM_000891.2:c.356_357insAAAATAA , LRG_328t1:c.356_357insAAAATAA | NP_000882.1:p.Ala121Ter | |
XM_011524779.1:c.356_357insAAAATAA | XP_011523081.1:p.Ala121Ter | |
NM_000891.3:c.356_357insAAAATAA MANE Select | NP_000882.1:p.Ala121Ter |