Canonical Allele Identifier: CA2091591470

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.52034999T= , CM000675.2:g.52034999T= GRCh38
NC_000013.10:g.52609135T= , CM000675.1:g.52609135T= GRCh37
NC_000013.9:g.51507136T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000647945.2:c.*1949A= (NEK5) ENSP00000497892.1:n.*1949A=
ENST00000684899.1:c.*1949A= (NEK5) MANE Select ENSP00000509632.1:n.*1949A=
ENST00000649708.2:c.275+15856T= (ALG11) ENSP00000497459.2:n.275+15856T=
ENST00000652502.1:n.4111A= (NEK5)
ENST00000679495.1:n.44+22537T= (ALG11)
ENST00000529080.5:n.2652A= (NEK5)
NM_001365552.1:c.*1949A= (NEK5) MANE Select NP_001352481.1:n.*1949A=