Canonical Allele Identifier: CA2189568061
Gene: HYKK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534613A= , CM000677.2:g.78534613A= GRCh38
NC_000015.9:g.78826955A= , CM000677.1:g.78826955A= GRCh37
NC_000015.8:g.76614010A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000388988.9:c.*943A= MANE Select ENSP00000373640.4:n.*943A=
ENST00000408962.6:c.662-2687A= ENSP00000386197.2:n.662-2687A=
ENST00000563233.2:c.662-2687A= ENSP00000454850.1:n.662-2687A=
ENST00000569878.5:c.2065A= ENSP00000455459.1:n.2065A=
NM_001083612.1:c.662-2687A= NP_001077081.1:n.662-2687A=
NM_001013619.3:c.*943A= NP_001013641.2:n.*943A=
NM_001013619.4:c.*943A= MANE Select NP_001013641.2:n.*943A=
NM_001083612.2:c.662-2687A= NP_001077081.1:n.662-2687A=
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