Canonical Allele Identifier: CA2731254913
Gene: HYKK HGNC NCBI

Linked Data

dbSNP Id: rs990282106
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534630C>G , CM000677.2:g.78534630C>G GRCh38
NC_000015.9:g.78826972C>G , CM000677.1:g.78826972C>G GRCh37
NC_000015.8:g.76614027C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000388988.9:c.*960C>G MANE Select ENSP00000373640.4:n.*960C>G
ENST00000408962.6:c.662-2670C>G ENSP00000386197.2:n.662-2670C>G
ENST00000563233.2:c.662-2670C>G ENSP00000454850.1:n.662-2670C>G
ENST00000569878.5:c.2082C>G ENSP00000455459.1:n.2082C>G
NM_001083612.1:c.662-2670C>G NP_001077081.1:n.662-2670C>G
NM_001013619.3:c.*960C>G NP_001013641.2:n.*960C>G
NM_001013619.4:c.*960C>G MANE Select NP_001013641.2:n.*960C>G
NM_001083612.2:c.662-2670C>G NP_001077081.1:n.662-2670C>G
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