Canonical Allele Identifier: CA2189557437
Gene: HYKK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78513535T= , CM000677.2:g.78513535T= GRCh38
NC_000015.9:g.78805877T= , CM000677.1:g.78805877T= GRCh37
NC_000015.8:g.76592932T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388988.9:c.337+110T= MANE Select ENSP00000373640.4:n.337+110T=
ENST00000388988.8:c.337+110T= ENSP00000373640.4:n.337+110T=
ENST00000408962.6:c.337+110T= ENSP00000386197.2:n.337+110T=
ENST00000563233.2:c.337+110T= ENSP00000454850.1:n.337+110T=
ENST00000566289.5:c.337+110T= ENSP00000456614.1:n.337+110T=
ENST00000566332.5:c.337+110T= ENSP00000457154.1:n.337+110T=
ENST00000569878.5:c.337+110T= ENSP00000455459.1:n.337+110T=
NM_001013619.2:c.337+110T= NP_001013641.2:n.337+110T=
NM_001083612.1:c.337+110T= NP_001077081.1:n.337+110T=
XM_011521231.1:c.337+110T= XP_011519533.1:n.337+110T=
XR_243078.3:n.432+110T=
NM_001013619.3:c.337+110T= NP_001013641.2:n.337+110T=
NM_001013619.4:c.337+110T= MANE Select NP_001013641.2:n.337+110T=
NM_001083612.2:c.337+110T= NP_001077081.1:n.337+110T=