Canonical Allele Identifier: CA2189568033
Gene: HYKK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534548_78534551delinsGCCT , CM000677.2:g.78534548_78534551delinsGCCT GRCh38
NC_000015.9:g.78826890_78826893delinsGCCT , CM000677.1:g.78826890_78826893delinsGCCT GRCh37
NC_000015.8:g.76613945_76613948delinsGCCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388988.9:c.*878_*881delinsGCCT MANE Select ENSP00000373640.4:n.*878_*881delinsGCCT
ENST00000408962.6:c.662-2752_662-2749delinsGCCT ENSP00000386197.2:n.662-2752_662-2749delinsGCCT
ENST00000563233.2:c.662-2752_662-2749delinsGCCT ENSP00000454850.1:n.662-2752_662-2749delinsGCCT
ENST00000569878.5:c.2000_2003delinsGCCT ENSP00000455459.1:n.2000_2003delinsGCCT
NM_001083612.1:c.662-2752_662-2749delinsGCCT NP_001077081.1:n.662-2752_662-2749delinsGCCT
NM_001013619.3:c.*878_*881delinsGCCT NP_001013641.2:n.*878_*881delinsGCCT
NM_001013619.4:c.*878_*881delinsGCCT MANE Select NP_001013641.2:n.*878_*881delinsGCCT
NM_001083612.2:c.662-2752_662-2749delinsGCCT NP_001077081.1:n.662-2752_662-2749delinsGCCT