Canonical Allele Identifier: CA2580089969
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2013895
ClinVar RCV Id: RCV002829749

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322684dup , CM000677.2:g.73322684dup GRCh38
NC_000015.9:g.73615025dup , CM000677.1:g.73615025dup GRCh37
NC_000015.8:g.71402078dup NCBI36
NG_009063.1:g.51585dup

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3413dup MANE Select ENSP00000261917.3:p.Gly1139TrpfsTer?
ENST00000261917.3:c.3413dup ENSP00000261917.3:p.Gly1139TrpfsTer?
NM_005477.2:c.3413dup NP_005468.1:p.Gly1139TrpfsTer?
XM_011521148.1:c.2195dup XP_011519450.1:p.Gly733TrpfsTer?
XM_011521148.2:c.2195dup XP_011519450.1:p.Gly733TrpfsTer?
NM_005477.3:c.3413dup MANE Select NP_005468.1:p.Gly1139TrpfsTer?