Canonical Allele Identifier: CA2629780398
Gene: HYKK HGNC NCBI

Linked Data

gnomAD v4: 15-78534585-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534585T>C , CM000677.2:g.78534585T>C GRCh38
NC_000015.9:g.78826927T>C , CM000677.1:g.78826927T>C GRCh37
NC_000015.8:g.76613982T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388988.9:c.*915T>C MANE Select ENSP00000373640.4:n.*915T>C
ENST00000408962.6:c.662-2715T>C ENSP00000386197.2:n.662-2715T>C
ENST00000563233.2:c.662-2715T>C ENSP00000454850.1:n.662-2715T>C
ENST00000569878.5:c.2037T>C ENSP00000455459.1:n.2037T>C
NM_001083612.1:c.662-2715T>C NP_001077081.1:n.662-2715T>C
NM_001013619.3:c.*915T>C NP_001013641.2:n.*915T>C
NM_001013619.4:c.*915T>C MANE Select NP_001013641.2:n.*915T>C
NM_001083612.2:c.662-2715T>C NP_001077081.1:n.662-2715T>C
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