Canonical Allele Identifier: CA2739269578
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2831795
ClinVar RCV Id: RCV003613932
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323489_73323506del , CM000677.2:g.73323489_73323506del GRCh38
NC_000015.9:g.73615830_73615847del , CM000677.1:g.73615830_73615847del GRCh37
NC_000015.8:g.71402883_71402900del NCBI36
NG_009063.1:g.50765_50782del

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2593_2610del MANE Select ENSP00000261917.3:p.Phe865_Gly870del
ENST00000261917.3:c.2593_2610del ENSP00000261917.3:p.Phe865_Gly870del
NM_005477.2:c.2593_2610del NP_005468.1:p.Phe865_Gly870del
XM_011521148.1:c.1375_1392del XP_011519450.1:p.Phe459_Gly464del
XM_011521148.2:c.1375_1392del XP_011519450.1:p.Phe459_Gly464del
NM_005477.3:c.2593_2610del MANE Select NP_005468.1:p.Phe865_Gly870del
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