Canonical Allele Identifier: CA715978365

Gene: HYKK

Linked Data

• dbSNP Id: rs1407052381
• gnomAD v4: 15-78513530-TGTG-T
• MyVariant Identifiers: chr15:g.78805873_78805875del (hg19) ; chr15:g.78513531_78513533del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78513533_78513535del , CM000677.2:g.78513533_78513535del	GRCh38
NC_000015.9:g.78805875_78805877del , CM000677.1:g.78805875_78805877del	GRCh37
NC_000015.8:g.76592930_76592932del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388988.9:c.337+108_337+110del MANE Select	ENSP00000373640.4:n.337+108_337+110del
ENST00000388988.8:c.337+108_337+110del	ENSP00000373640.4:n.337+108_337+110del
ENST00000408962.6:c.337+108_337+110del	ENSP00000386197.2:n.337+108_337+110del
ENST00000563233.2:c.337+108_337+110del	ENSP00000454850.1:n.337+108_337+110del
ENST00000566289.5:c.337+108_337+110del	ENSP00000456614.1:n.337+108_337+110del
ENST00000566332.5:c.337+108_337+110del	ENSP00000457154.1:n.337+108_337+110del
ENST00000569878.5:c.337+108_337+110del	ENSP00000455459.1:n.337+108_337+110del
NM_001013619.2:c.337+108_337+110del	NP_001013641.2:n.337+108_337+110del
NM_001083612.1:c.337+108_337+110del	NP_001077081.1:n.337+108_337+110del
XM_011521231.1:c.337+108_337+110del	XP_011519533.1:n.337+108_337+110del
XR_243078.3:n.432+108_432+110del
NM_001013619.3:c.337+108_337+110del	NP_001013641.2:n.337+108_337+110del
NM_001013619.4:c.337+108_337+110del MANE Select	NP_001013641.2:n.337+108_337+110del
NM_001083612.2:c.337+108_337+110del	NP_001077081.1:n.337+108_337+110del