Canonical Allele Identifier: CA2091591455

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.52034973_52034974delinsCA , CM000675.2:g.52034973_52034974delinsCA GRCh38
NC_000013.10:g.52609109_52609110delinsCA , CM000675.1:g.52609109_52609110delinsCA GRCh37
NC_000013.9:g.51507110_51507111delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000647945.2:c.*1974_*1975delinsTG (NEK5) ENSP00000497892.1:n.*1974_*1975delinsTG
ENST00000684899.1:c.*1974_*1975delinsTG (NEK5) MANE Select ENSP00000509632.1:n.*1974_*1975delinsTG
ENST00000649708.2:c.275+15830_275+15831delinsCA (ALG11) ENSP00000497459.2:n.275+15830_275+15831de...
ENST00000652502.1:n.4136_4137delinsTG (NEK5)
ENST00000679495.1:n.44+22511_44+22512delinsCA (ALG11)
ENST00000529080.5:n.2677_2678delinsTG (NEK5)
NM_001365552.1:c.*1974_*1975delinsTG (NEK5) MANE Select NP_001352481.1:n.*1974_*1975delinsTG