Canonical Allele Identifier: CA2629780352
Gene: HYKK HGNC NCBI

Linked Data

gnomAD v4: 15-78534525-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534525A>G , CM000677.2:g.78534525A>G GRCh38
NC_000015.9:g.78826867A>G , CM000677.1:g.78826867A>G GRCh37
NC_000015.8:g.76613922A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388988.9:c.*855A>G MANE Select ENSP00000373640.4:n.*855A>G
ENST00000408962.6:c.662-2775A>G ENSP00000386197.2:n.662-2775A>G
ENST00000563233.2:c.662-2775A>G ENSP00000454850.1:n.662-2775A>G
ENST00000569878.5:c.1977A>G ENSP00000455459.1:n.1977A>G
NM_001083612.1:c.662-2775A>G NP_001077081.1:n.662-2775A>G
NM_001013619.3:c.*855A>G NP_001013641.2:n.*855A>G
NM_001013619.4:c.*855A>G MANE Select NP_001013641.2:n.*855A>G
NM_001083612.2:c.662-2775A>G NP_001077081.1:n.662-2775A>G
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