Canonical Allele Identifier: CA2091591523

Linked Data

dbSNP Id: rs949535566

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.52035091C>A , CM000675.2:g.52035091C>A GRCh38
NC_000013.10:g.52609227C>A , CM000675.1:g.52609227C>A GRCh37
NC_000013.9:g.51507228C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000647945.2:c.*1857G>T (NEK5) ENSP00000497892.1:n.*1857G>T
ENST00000684899.1:c.*1857G>T (NEK5) MANE Select ENSP00000509632.1:n.*1857G>T
ENST00000649708.2:c.275+15948C>A (ALG11) ENSP00000497459.2:n.275+15948C>A
ENST00000652502.1:n.4019G>T (NEK5)
ENST00000679495.1:n.44+22629C>A (ALG11)
ENST00000529080.5:n.2560G>T (NEK5)
NM_001365552.1:c.*1857G>T (NEK5) MANE Select NP_001352481.1:n.*1857G>T