Canonical Allele Identifier: CA2091591458

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.52034978C= , CM000675.2:g.52034978C= GRCh38
NC_000013.10:g.52609114C= , CM000675.1:g.52609114C= GRCh37
NC_000013.9:g.51507115C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000647945.2:c.*1970G= (NEK5) ENSP00000497892.1:n.*1970G=
ENST00000684899.1:c.*1970G= (NEK5) MANE Select ENSP00000509632.1:n.*1970G=
ENST00000649708.2:c.275+15835C= (ALG11) ENSP00000497459.2:n.275+15835C=
ENST00000652502.1:n.4132G= (NEK5)
ENST00000679495.1:n.44+22516C= (ALG11)
ENST00000529080.5:n.2673G= (NEK5)
NM_001365552.1:c.*1970G= (NEK5) MANE Select NP_001352481.1:n.*1970G=