Canonical Allele Identifier: CA2740096730
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3006239
ClinVar RCV Id: RCV003866390
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322869_73322871del , CM000677.2:g.73322869_73322871del GRCh38
NC_000015.9:g.73615210_73615212del , CM000677.1:g.73615210_73615212del GRCh37
NC_000015.8:g.71402263_71402265del NCBI36
NG_009063.1:g.51395_51397del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3223_3225del MANE Select ENSP00000261917.3:p.Thr1075del
ENST00000261917.3:c.3223_3225del ENSP00000261917.3:p.Thr1075del
NM_005477.2:c.3223_3225del NP_005468.1:p.Thr1075del
XM_011521148.1:c.2005_2007del XP_011519450.1:p.Thr669del
XM_011521148.2:c.2005_2007del XP_011519450.1:p.Thr669del
NM_005477.3:c.3223_3225del MANE Select NP_005468.1:p.Thr1075del
Search 100 bp 5'
Search 100 bp 3'