HGVS | Genome Assembly |
---|---|
NC_000013.11:g.52035091C>T , CM000675.2:g.52035091C>T | GRCh38 |
NC_000013.10:g.52609227C>T , CM000675.1:g.52609227C>T | GRCh37 |
NC_000013.9:g.51507228C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647945.2:c.*1857G>A (NEK5) | ENSP00000497892.1:n.*1857G>A | |
ENST00000684899.1:c.*1857G>A (NEK5) MANE Select | ENSP00000509632.1:n.*1857G>A | |
ENST00000649708.2:c.275+15948C>T (ALG11) | ENSP00000497459.2:n.275+15948C>T | |
ENST00000652502.1:n.4019G>A (NEK5) | ||
ENST00000679495.1:n.44+22629C>T (ALG11) | ||
ENST00000529080.5:n.2560G>A (NEK5) | ||
NM_001365552.1:c.*1857G>A (NEK5) MANE Select | NP_001352481.1:n.*1857G>A |