Canonical Allele Identifier: CA2091591480

Linked Data

dbSNP Id: rs1954347718

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.52035031C>T , CM000675.2:g.52035031C>T GRCh38
NC_000013.10:g.52609167C>T , CM000675.1:g.52609167C>T GRCh37
NC_000013.9:g.51507168C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000647945.2:c.*1917G>A (NEK5) ENSP00000497892.1:n.*1917G>A
ENST00000684899.1:c.*1917G>A (NEK5) MANE Select ENSP00000509632.1:n.*1917G>A
ENST00000649708.2:c.275+15888C>T (ALG11) ENSP00000497459.2:n.275+15888C>T
ENST00000652502.1:n.4079G>A (NEK5)
ENST00000679495.1:n.44+22569C>T (ALG11)
ENST00000529080.5:n.2620G>A (NEK5)
NM_001365552.1:c.*1917G>A (NEK5) MANE Select NP_001352481.1:n.*1917G>A