Canonical Allele Identifier: CA2629780422
Gene: HYKK HGNC NCBI

Linked Data

gnomAD v4: 15-78534640-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78534640G>T , CM000677.2:g.78534640G>T GRCh38
NC_000015.9:g.78826982G>T , CM000677.1:g.78826982G>T GRCh37
NC_000015.8:g.76614037G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388988.9:c.*970G>T MANE Select ENSP00000373640.4:n.*970G>T
ENST00000408962.6:c.662-2660G>T ENSP00000386197.2:n.662-2660G>T
ENST00000563233.2:c.662-2660G>T ENSP00000454850.1:n.662-2660G>T
ENST00000569878.5:c.2092G>T ENSP00000455459.1:n.2092G>T
NM_001083612.1:c.662-2660G>T NP_001077081.1:n.662-2660G>T
NM_001013619.3:c.*970G>T NP_001013641.2:n.*970G>T
NM_001013619.4:c.*970G>T MANE Select NP_001013641.2:n.*970G>T
NM_001083612.2:c.662-2660G>T NP_001077081.1:n.662-2660G>T
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