Canonical Allele Identifier: CA2629777694

Gene: HYKK

Linked Data

• gnomAD v4: 15-78513552-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78513552C>A , CM000677.2:g.78513552C>A	GRCh38
NC_000015.9:g.78805894C>A , CM000677.1:g.78805894C>A	GRCh37
NC_000015.8:g.76592949C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388988.9:c.337+127C>A MANE Select	ENSP00000373640.4:n.337+127C>A
ENST00000388988.8:c.337+127C>A	ENSP00000373640.4:n.337+127C>A
ENST00000408962.6:c.337+127C>A	ENSP00000386197.2:n.337+127C>A
ENST00000563233.2:c.337+127C>A	ENSP00000454850.1:n.337+127C>A
ENST00000566289.5:c.337+127C>A	ENSP00000456614.1:n.337+127C>A
ENST00000566332.5:c.337+127C>A	ENSP00000457154.1:n.337+127C>A
ENST00000569878.5:c.337+127C>A	ENSP00000455459.1:n.337+127C>A
NM_001013619.2:c.337+127C>A	NP_001013641.2:n.337+127C>A
NM_001083612.1:c.337+127C>A	NP_001077081.1:n.337+127C>A
XM_011521231.1:c.337+127C>A	XP_011519533.1:n.337+127C>A
XR_243078.3:n.432+127C>A
NM_001013619.3:c.337+127C>A	NP_001013641.2:n.337+127C>A
NM_001013619.4:c.337+127C>A MANE Select	NP_001013641.2:n.337+127C>A
NM_001083612.2:c.337+127C>A	NP_001077081.1:n.337+127C>A