Canonical Allele Identifier: CA2629780420
Gene: HYKK HGNC NCBI

Linked Data

gnomAD v4: 15-78534636-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534636A>T , CM000677.2:g.78534636A>T GRCh38
NC_000015.9:g.78826978A>T , CM000677.1:g.78826978A>T GRCh37
NC_000015.8:g.76614033A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000388988.9:c.*966A>T MANE Select ENSP00000373640.4:n.*966A>T
ENST00000408962.6:c.662-2664A>T ENSP00000386197.2:n.662-2664A>T
ENST00000563233.2:c.662-2664A>T ENSP00000454850.1:n.662-2664A>T
ENST00000569878.5:c.2088A>T ENSP00000455459.1:n.2088A>T
NM_001083612.1:c.662-2664A>T NP_001077081.1:n.662-2664A>T
NM_001013619.3:c.*966A>T NP_001013641.2:n.*966A>T
NM_001013619.4:c.*966A>T MANE Select NP_001013641.2:n.*966A>T
NM_001083612.2:c.662-2664A>T NP_001077081.1:n.662-2664A>T
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