Canonical Allele Identifier: CA491610710

Gene: HYKK

Linked Data

• MyVariant Identifiers: chr15:g.78805766A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78513424A>C , CM000677.2:g.78513424A>C	GRCh38
NC_000015.9:g.78805766A>C , CM000677.1:g.78805766A>C	GRCh37
NC_000015.8:g.76592821A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388988.9:c.336A>C MANE Select	ENSP00000373640.4:p.Val112=
ENST00000388988.8:c.336A>C	ENSP00000373640.4:p.Val112=
ENST00000408962.6:c.336A>C	ENSP00000386197.2:p.Val112=
ENST00000563233.2:c.336A>C	ENSP00000454850.1:p.Val112=
ENST00000566289.5:c.336A>C	ENSP00000456614.1:p.Val112=
ENST00000566332.5:c.336A>C	ENSP00000457154.1:p.Val112=
ENST00000569878.5:c.336A>C	ENSP00000455459.1:p.Val112=
NM_001013619.2:c.336A>C	NP_001013641.2:p.Val112=
NM_001083612.1:c.336A>C	NP_001077081.1:p.Val112=
XM_011521231.1:c.336A>C	XP_011519533.1:p.Val112=
XR_243078.3:n.431A>C
NM_001013619.3:c.336A>C	NP_001013641.2:p.Val112=
NM_001013619.4:c.336A>C MANE Select	NP_001013641.2:p.Val112=
NM_001083612.2:c.336A>C	NP_001077081.1:p.Val112=