Canonical Allele Identifier: CA2189568058

Gene: HYKK

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78534606T= , CM000677.2:g.78534606T=	GRCh38
NC_000015.9:g.78826948T= , CM000677.1:g.78826948T=	GRCh37
NC_000015.8:g.76614003T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388988.9:c.*936T= MANE Select	ENSP00000373640.4:n.*936T=
ENST00000408962.6:c.662-2694T=	ENSP00000386197.2:n.662-2694T=
ENST00000563233.2:c.662-2694T=	ENSP00000454850.1:n.662-2694T=
ENST00000569878.5:c.2058T=	ENSP00000455459.1:n.2058T=
NM_001083612.1:c.662-2694T=	NP_001077081.1:n.662-2694T=
NM_001013619.3:c.*936T=	NP_001013641.2:n.*936T=
NM_001013619.4:c.*936T= MANE Select	NP_001013641.2:n.*936T=
NM_001083612.2:c.662-2694T=	NP_001077081.1:n.662-2694T=