Canonical Allele Identifier: CA2189568018
Gene: HYKK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534521G= , CM000677.2:g.78534521G= GRCh38
NC_000015.9:g.78826863G= , CM000677.1:g.78826863G= GRCh37
NC_000015.8:g.76613918G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388988.9:c.*851G= MANE Select ENSP00000373640.4:n.*851G=
ENST00000408962.6:c.662-2779G= ENSP00000386197.2:n.662-2779G=
ENST00000563233.2:c.662-2779G= ENSP00000454850.1:n.662-2779G=
ENST00000569878.5:c.1973G= ENSP00000455459.1:n.1973G=
NM_001083612.1:c.662-2779G= NP_001077081.1:n.662-2779G=
NM_001013619.3:c.*851G= NP_001013641.2:n.*851G=
NM_001013619.4:c.*851G= MANE Select NP_001013641.2:n.*851G=
NM_001083612.2:c.662-2779G= NP_001077081.1:n.662-2779G=
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