Canonical Allele Identifier: CA7648826
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 518849
dbSNP Id: rs746402732

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322679del , CM000677.2:g.73322679del GRCh38
NC_000015.9:g.73615020del , CM000677.1:g.73615020del GRCh37
NC_000015.8:g.71402073del NCBI36
NG_009063.1:g.51586del

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3414del MANE Select ENSP00000261917.3:p.Arg1140GlyfsTer?
ENST00000261917.3:c.3414del ENSP00000261917.3:p.Arg1140GlyfsTer?
NM_005477.2:c.3414del NP_005468.1:p.Arg1140GlyfsTer?
XM_011521148.1:c.2196del XP_011519450.1:p.Arg734GlyfsTer?
XM_011521148.2:c.2196del XP_011519450.1:p.Arg734GlyfsTer?
NM_005477.3:c.3414del MANE Select NP_005468.1:p.Arg1140GlyfsTer?