Canonical Allele Identifier: CA273904749
Gene: HYKK HGNC NCBI

Linked Data

dbSNP Id: rs1008186482
gnomAD v2: 15-78826883-G-A
gnomAD v3: 15-78534541-G-A
gnomAD v4: 15-78534541-G-A
COSMIC: COSN6073317
MyVariant Identifiers: chr15:g.78826883G>A (hg19) chr15:g.78534541G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534541G>A , CM000677.2:g.78534541G>A GRCh38
NC_000015.9:g.78826883G>A , CM000677.1:g.78826883G>A GRCh37
NC_000015.8:g.76613938G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388988.9:c.*871G>A MANE Select ENSP00000373640.4:n.*871G>A
ENST00000408962.6:c.662-2759G>A ENSP00000386197.2:n.662-2759G>A
ENST00000563233.2:c.662-2759G>A ENSP00000454850.1:n.662-2759G>A
ENST00000569878.5:c.1993G>A ENSP00000455459.1:n.1993G>A
NM_001083612.1:c.662-2759G>A NP_001077081.1:n.662-2759G>A
NM_001013619.3:c.*871G>A NP_001013641.2:n.*871G>A
NM_001013619.4:c.*871G>A MANE Select NP_001013641.2:n.*871G>A
NM_001083612.2:c.662-2759G>A NP_001077081.1:n.662-2759G>A
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