Canonical Allele Identifier: CA2189557495

Gene: HYKK

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78513577T= , CM000677.2:g.78513577T=	GRCh38
NC_000015.9:g.78805919T= , CM000677.1:g.78805919T=	GRCh37
NC_000015.8:g.76592974T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388988.9:c.337+152T= MANE Select	ENSP00000373640.4:n.337+152T=
ENST00000388988.8:c.337+152T=	ENSP00000373640.4:n.337+152T=
ENST00000408962.6:c.337+152T=	ENSP00000386197.2:n.337+152T=
ENST00000563233.2:c.337+152T=	ENSP00000454850.1:n.337+152T=
ENST00000566289.5:c.337+152T=	ENSP00000456614.1:n.337+152T=
ENST00000566332.5:c.337+152T=	ENSP00000457154.1:n.337+152T=
ENST00000569878.5:c.337+152T=	ENSP00000455459.1:n.337+152T=
NM_001013619.2:c.337+152T=	NP_001013641.2:n.337+152T=
NM_001083612.1:c.337+152T=	NP_001077081.1:n.337+152T=
XM_011521231.1:c.337+152T=	XP_011519533.1:n.337+152T=
XR_243078.3:n.432+152T=
NM_001013619.3:c.337+152T=	NP_001013641.2:n.337+152T=
NM_001013619.4:c.337+152T= MANE Select	NP_001013641.2:n.337+152T=
NM_001083612.2:c.337+152T=	NP_001077081.1:n.337+152T=