Canonical Allele Identifier: CA2091591566

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.52035169G= , CM000675.2:g.52035169G= GRCh38
NC_000013.10:g.52609305G= , CM000675.1:g.52609305G= GRCh37
NC_000013.9:g.51507306G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000647945.2:c.*1779C= (NEK5) ENSP00000497892.1:n.*1779C=
ENST00000684899.1:c.*1779C= (NEK5) MANE Select ENSP00000509632.1:n.*1779C=
ENST00000649708.2:c.275+16026G= (ALG11) ENSP00000497459.2:n.275+16026G=
ENST00000652502.1:n.3941C= (NEK5)
ENST00000679495.1:n.44+22707G= (ALG11)
ENST00000529080.5:n.2482C= (NEK5)
NM_001365552.1:c.*1779C= (NEK5) MANE Select NP_001352481.1:n.*1779C=