Canonical Allele Identifier: CA715978427

Gene: HYKK

Linked Data

• dbSNP Id: rs1251989764
• gnomAD v3: 15-78513663-TG-T
• gnomAD v4: 15-78513663-TG-T
• MyVariant Identifiers: chr15:g.78806006del (hg19) ; chr15:g.78513664del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78513665del , CM000677.2:g.78513665del	GRCh38
NC_000015.9:g.78806007del , CM000677.1:g.78806007del	GRCh37
NC_000015.8:g.76593062del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388988.9:c.337+240del MANE Select	ENSP00000373640.4:n.337+240del
ENST00000388988.8:c.337+240del	ENSP00000373640.4:n.337+240del
ENST00000408962.6:c.337+240del	ENSP00000386197.2:n.337+240del
ENST00000563233.2:c.337+240del	ENSP00000454850.1:n.337+240del
ENST00000566289.5:c.337+240del	ENSP00000456614.1:n.337+240del
ENST00000566332.5:c.337+240del	ENSP00000457154.1:n.337+240del
ENST00000569878.5:c.337+240del	ENSP00000455459.1:n.337+240del
NM_001013619.2:c.337+240del	NP_001013641.2:n.337+240del
NM_001083612.1:c.337+240del	NP_001077081.1:n.337+240del
XM_011521231.1:c.337+240del	XP_011519533.1:n.337+240del
XR_243078.3:n.432+240del
NM_001013619.3:c.337+240del	NP_001013641.2:n.337+240del
NM_001013619.4:c.337+240del MANE Select	NP_001013641.2:n.337+240del
NM_001083612.2:c.337+240del	NP_001077081.1:n.337+240del