Canonical Allele Identifier: CA2629780417
Gene: HYKK HGNC NCBI

Linked Data

gnomAD v4: 15-78534628-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534628T>A , CM000677.2:g.78534628T>A GRCh38
NC_000015.9:g.78826970T>A , CM000677.1:g.78826970T>A GRCh37
NC_000015.8:g.76614025T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000388988.9:c.*958T>A MANE Select ENSP00000373640.4:n.*958T>A
ENST00000408962.6:c.662-2672T>A ENSP00000386197.2:n.662-2672T>A
ENST00000563233.2:c.662-2672T>A ENSP00000454850.1:n.662-2672T>A
ENST00000569878.5:c.2080T>A ENSP00000455459.1:n.2080T>A
NM_001083612.1:c.662-2672T>A NP_001077081.1:n.662-2672T>A
NM_001013619.3:c.*958T>A NP_001013641.2:n.*958T>A
NM_001013619.4:c.*958T>A MANE Select NP_001013641.2:n.*958T>A
NM_001083612.2:c.662-2672T>A NP_001077081.1:n.662-2672T>A
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