Canonical Allele Identifier: CA2629780388
Gene: HYKK HGNC NCBI

Linked Data

gnomAD v4: 15-78534571-AC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534573del , CM000677.2:g.78534573del GRCh38
NC_000015.9:g.78826915del , CM000677.1:g.78826915del GRCh37
NC_000015.8:g.76613970del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388988.9:c.*903del MANE Select ENSP00000373640.4:n.*903del
ENST00000408962.6:c.662-2727del ENSP00000386197.2:n.662-2727del
ENST00000563233.2:c.662-2727del ENSP00000454850.1:n.662-2727del
ENST00000569878.5:c.2025del ENSP00000455459.1:n.2025del
NM_001083612.1:c.662-2727del NP_001077081.1:n.662-2727del
NM_001013619.3:c.*903del NP_001013641.2:n.*903del
NM_001013619.4:c.*903del MANE Select NP_001013641.2:n.*903del
NM_001083612.2:c.662-2727del NP_001077081.1:n.662-2727del
Search 100 bp 5'
Search 100 bp 3'