Canonical Allele Identifier: CA2629780387
Gene: HYKK HGNC NCBI

Linked Data

gnomAD v4: 15-78534568-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534568C>A , CM000677.2:g.78534568C>A GRCh38
NC_000015.9:g.78826910C>A , CM000677.1:g.78826910C>A GRCh37
NC_000015.8:g.76613965C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388988.9:c.*898C>A MANE Select ENSP00000373640.4:n.*898C>A
ENST00000408962.6:c.662-2732C>A ENSP00000386197.2:n.662-2732C>A
ENST00000563233.2:c.662-2732C>A ENSP00000454850.1:n.662-2732C>A
ENST00000569878.5:c.2020C>A ENSP00000455459.1:n.2020C>A
NM_001083612.1:c.662-2732C>A NP_001077081.1:n.662-2732C>A
NM_001013619.3:c.*898C>A NP_001013641.2:n.*898C>A
NM_001013619.4:c.*898C>A MANE Select NP_001013641.2:n.*898C>A
NM_001083612.2:c.662-2732C>A NP_001077081.1:n.662-2732C>A
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