Canonical Allele Identifier: CA273904820
Gene: HYKK HGNC NCBI

Linked Data

dbSNP Id: rs1034328479
gnomAD v3: 15-78534608-T-TA
gnomAD v4: 15-78534608-T-TA
MyVariant Identifiers: chr15:g.78826950_78826951insA (hg19) chr15:g.78534608_78534609insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534613dup , CM000677.2:g.78534613dup GRCh38
NC_000015.9:g.78826955dup , CM000677.1:g.78826955dup GRCh37
NC_000015.8:g.76614010dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388988.9:c.*943dup MANE Select ENSP00000373640.4:n.*943dup
ENST00000408962.6:c.662-2687dup ENSP00000386197.2:n.662-2687dup
ENST00000563233.2:c.662-2687dup ENSP00000454850.1:n.662-2687dup
ENST00000569878.5:c.2065dup ENSP00000455459.1:n.2065dup
NM_001083612.1:c.662-2687dup NP_001077081.1:n.662-2687dup
NM_001013619.3:c.*943dup NP_001013641.2:n.*943dup
NM_001013619.4:c.*943dup MANE Select NP_001013641.2:n.*943dup
NM_001083612.2:c.662-2687dup NP_001077081.1:n.662-2687dup
Search 100 bp 5'
Search 100 bp 3'