Canonical Allele Identifier: CA2623122368

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.52035046C>A , CM000675.2:g.52035046C>A GRCh38
NC_000013.10:g.52609182C>A , CM000675.1:g.52609182C>A GRCh37
NC_000013.9:g.51507183C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000647945.2:c.*1902G>T (NEK5) ENSP00000497892.1:n.*1902G>T
ENST00000684899.1:c.*1902G>T (NEK5) MANE Select ENSP00000509632.1:n.*1902G>T
ENST00000649708.2:c.275+15903C>A (ALG11) ENSP00000497459.2:n.275+15903C>A
ENST00000652502.1:n.4064G>T (NEK5)
ENST00000679495.1:n.44+22584C>A (ALG11)
ENST00000529080.5:n.2605G>T (NEK5)
NM_001365552.1:c.*1902G>T (NEK5) MANE Select NP_001352481.1:n.*1902G>T