Canonical Allele Identifier: CA2731361402
Gene: HYKK HGNC NCBI

Linked Data

dbSNP Id: rs2141366751
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534620A>G , CM000677.2:g.78534620A>G GRCh38
NC_000015.9:g.78826962A>G , CM000677.1:g.78826962A>G GRCh37
NC_000015.8:g.76614017A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000388988.9:c.*950A>G MANE Select ENSP00000373640.4:n.*950A>G
ENST00000408962.6:c.662-2680A>G ENSP00000386197.2:n.662-2680A>G
ENST00000563233.2:c.662-2680A>G ENSP00000454850.1:n.662-2680A>G
ENST00000569878.5:c.2072A>G ENSP00000455459.1:n.2072A>G
NM_001083612.1:c.662-2680A>G NP_001077081.1:n.662-2680A>G
NM_001013619.3:c.*950A>G NP_001013641.2:n.*950A>G
NM_001013619.4:c.*950A>G MANE Select NP_001013641.2:n.*950A>G
NM_001083612.2:c.662-2680A>G NP_001077081.1:n.662-2680A>G
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