HGVS | Genome Assembly |
---|---|
NC_000017.11:g.40867027del , CM000679.2:g.40867027del | GRCh38 |
NC_000017.10:g.39023279del , CM000679.1:g.39023279del | GRCh37 |
NC_000017.9:g.36276805del | NCBI36 |
NG_008077.1:g.5188del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251643.5:c.164del MANE Select | ENSP00000251643.4:p.Gly55GlufsTer? | |
ENST00000647902.1:c.164del | ENSP00000497770.1:p.Gly55GlufsTer20 | |
ENST00000251643.4:c.164del | ENSP00000251643.4:p.Gly55GlufsTer? | |
NM_000223.3:c.164del | NP_000214.1:p.Gly55GlufsTer? | |
XR_934754.1:n.1500+16167del | ||
XR_934754.2:n.2008+16167del | ||
NM_000223.4:c.164del MANE Select | NP_000214.1:p.Gly55GlufsTer? |