Canonical Allele Identifier: CA2189568066

Gene: HYKK

Linked Data

• dbSNP Id: rs1596036916

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78534625A>G , CM000677.2:g.78534625A>G	GRCh38
NC_000015.9:g.78826967A>G , CM000677.1:g.78826967A>G	GRCh37
NC_000015.8:g.76614022A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388988.9:c.*955A>G MANE Select	ENSP00000373640.4:n.*955A>G
ENST00000408962.6:c.662-2675A>G	ENSP00000386197.2:n.662-2675A>G
ENST00000563233.2:c.662-2675A>G	ENSP00000454850.1:n.662-2675A>G
ENST00000569878.5:c.2077A>G	ENSP00000455459.1:n.2077A>G
NM_001083612.1:c.662-2675A>G	NP_001077081.1:n.662-2675A>G
NM_001013619.3:c.*955A>G	NP_001013641.2:n.*955A>G
NM_001013619.4:c.*955A>G MANE Select	NP_001013641.2:n.*955A>G
NM_001083612.2:c.662-2675A>G	NP_001077081.1:n.662-2675A>G