Canonical Allele Identifier: CA2629780360
Gene: HYKK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534534A>G , CM000677.2:g.78534534A>G GRCh38
NC_000015.9:g.78826876A>G , CM000677.1:g.78826876A>G GRCh37
NC_000015.8:g.76613931A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388988.9:c.*864A>G MANE Select ENSP00000373640.4:n.*864A>G
ENST00000408962.6:c.662-2766A>G ENSP00000386197.2:n.662-2766A>G
ENST00000563233.2:c.662-2766A>G ENSP00000454850.1:n.662-2766A>G
ENST00000569878.5:c.1986A>G ENSP00000455459.1:n.1986A>G
NM_001083612.1:c.662-2766A>G NP_001077081.1:n.662-2766A>G
NM_001013619.3:c.*864A>G NP_001013641.2:n.*864A>G
NM_001013619.4:c.*864A>G MANE Select NP_001013641.2:n.*864A>G
NM_001083612.2:c.662-2766A>G NP_001077081.1:n.662-2766A>G