Canonical Allele Identifier: CA619230763

Gene: HYKK

Linked Data

• dbSNP Id: rs1316707875
• gnomAD v2: 15-78826977-TAGA-T
• gnomAD v3: 15-78534635-TAGA-T
• gnomAD v4: 15-78534635-TAGA-T
• MyVariant Identifiers: chr15:g.78826978_78826980del (hg19) ; chr15:g.78534636_78534638del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78534641_78534643del , CM000677.2:g.78534641_78534643del	GRCh38
NC_000015.9:g.78826983_78826985del , CM000677.1:g.78826983_78826985del	GRCh37
NC_000015.8:g.76614038_76614040del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000388988.9:c.*971_*973del MANE Select	ENSP00000373640.4:n.*971_*973del
ENST00000408962.6:c.662-2659_662-2657del	ENSP00000386197.2:n.662-2659_662-2657del
ENST00000563233.2:c.662-2659_662-2657del	ENSP00000454850.1:n.662-2659_662-2657del
ENST00000569878.5:c.2093_2095del	ENSP00000455459.1:n.2093_2095del
NM_001083612.1:c.662-2659_662-2657del	NP_001077081.1:n.662-2659_662-2657del
NM_001013619.3:c.*971_*973del	NP_001013641.2:n.*971_*973del
NM_001013619.4:c.*971_*973del MANE Select	NP_001013641.2:n.*971_*973del
NM_001083612.2:c.662-2659_662-2657del	NP_001077081.1:n.662-2659_662-2657del