Canonical Allele Identifier: CA2189568040
Gene: HYKK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534570C= , CM000677.2:g.78534570C= GRCh38
NC_000015.9:g.78826912C= , CM000677.1:g.78826912C= GRCh37
NC_000015.8:g.76613967C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388988.9:c.*900C= MANE Select ENSP00000373640.4:n.*900C=
ENST00000408962.6:c.662-2730C= ENSP00000386197.2:n.662-2730C=
ENST00000563233.2:c.662-2730C= ENSP00000454850.1:n.662-2730C=
ENST00000569878.5:c.2022C= ENSP00000455459.1:n.2022C=
NM_001083612.1:c.662-2730C= NP_001077081.1:n.662-2730C=
NM_001013619.3:c.*900C= NP_001013641.2:n.*900C=
NM_001013619.4:c.*900C= MANE Select NP_001013641.2:n.*900C=
NM_001083612.2:c.662-2730C= NP_001077081.1:n.662-2730C=
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