HGVS | Genome Assembly |
---|---|
NC_000013.11:g.113735281_113735284del , CM000675.2:g.113735281_113735284del | GRCh38 |
NC_000013.10:g.114438254_114438257del , CM000675.1:g.114438254_114438257del | GRCh37 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000335678.7:c.1610_1613del MANE Select | ENSP00000334876.5:p.Asp537ValfsTer7 | |
ENST00000335678.6:c.1610_1613del | ENSP00000334876.5:p.Asp537ValfsTer7 | |
ENST00000606140.1:n.807_810del | ||
NM_002929.2:c.1610_1613del | NP_002920.1:p.Asp537ValfsTer7 | |
XM_017020684.1:c.905_908del | XP_016876173.1:p.Asp302ValfsTer7 | |
NM_002929.3:c.1610_1613del MANE Select | NP_002920.1:p.Asp537ValfsTer7 |