Canonical Allele Identifier: CA2189568098

Gene: HYKK

Linked Data

• dbSNP Id: rs2050192074

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78534717_78534718insAG , CM000677.2:g.78534717_78534718insAG	GRCh38
NC_000015.9:g.78827059_78827060insAG , CM000677.1:g.78827059_78827060insAG	GRCh37
NC_000015.8:g.76614114_76614115insAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388988.9:c.*1047_*1048insAG MANE Select	ENSP00000373640.4:n.*1047_*1048insAG
ENST00000408962.6:c.662-2583_662-2582insAG	ENSP00000386197.2:n.662-2583_662-2582insAG
ENST00000563233.2:c.662-2583_662-2582insAG	ENSP00000454850.1:n.662-2583_662-2582insAG
ENST00000569878.5:c.2169_2170insAG	ENSP00000455459.1:n.2169_2170insAG
NM_001083612.1:c.662-2583_662-2582insAG	NP_001077081.1:n.662-2583_662-2582insAG
NM_001013619.3:c.*1047_*1048insAG	NP_001013641.2:n.*1047_*1048insAG
NM_001013619.4:c.*1047_*1048insAG MANE Select	NP_001013641.2:n.*1047_*1048insAG
NM_001083612.2:c.662-2583_662-2582insAG	NP_001077081.1:n.662-2583_662-2582insAG