Canonical Allele Identifier: CA2189568062
Gene: HYKK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534616T= , CM000677.2:g.78534616T= GRCh38
NC_000015.9:g.78826958T= , CM000677.1:g.78826958T= GRCh37
NC_000015.8:g.76614013T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000388988.9:c.*946T= MANE Select ENSP00000373640.4:n.*946T=
ENST00000408962.6:c.662-2684T= ENSP00000386197.2:n.662-2684T=
ENST00000563233.2:c.662-2684T= ENSP00000454850.1:n.662-2684T=
ENST00000569878.5:c.2068T= ENSP00000455459.1:n.2068T=
NM_001083612.1:c.662-2684T= NP_001077081.1:n.662-2684T=
NM_001013619.3:c.*946T= NP_001013641.2:n.*946T=
NM_001013619.4:c.*946T= MANE Select NP_001013641.2:n.*946T=
NM_001083612.2:c.662-2684T= NP_001077081.1:n.662-2684T=
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