Canonical Allele Identifier: CA2629780458
Gene: HYKK HGNC NCBI

Linked Data

gnomAD v4: 15-78534731-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534731G>A , CM000677.2:g.78534731G>A GRCh38
NC_000015.9:g.78827073G>A , CM000677.1:g.78827073G>A GRCh37
NC_000015.8:g.76614128G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388988.9:c.*1061G>A MANE Select ENSP00000373640.4:n.*1061G>A
ENST00000408962.6:c.662-2569G>A ENSP00000386197.2:n.662-2569G>A
ENST00000563233.2:c.662-2569G>A ENSP00000454850.1:n.662-2569G>A
ENST00000569878.5:c.2183G>A ENSP00000455459.1:n.2183G>A
NM_001083612.1:c.662-2569G>A NP_001077081.1:n.662-2569G>A
NM_001013619.3:c.*1061G>A NP_001013641.2:n.*1061G>A
NM_001013619.4:c.*1061G>A MANE Select NP_001013641.2:n.*1061G>A
NM_001083612.2:c.662-2569G>A NP_001077081.1:n.662-2569G>A
Search 100 bp 5'
Search 100 bp 3'