Canonical Allele Identifier: CA2629370523
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322587_73322590del , CM000677.2:g.73322587_73322590del GRCh38
NC_000015.9:g.73614928_73614931del , CM000677.1:g.73614928_73614931del GRCh37
NC_000015.8:g.71401981_71401984del NCBI36
NG_009063.1:g.51675_51678del

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3503_3506del MANE Select ENSP00000261917.3:p.Phe1168TrpfsTer12
ENST00000261917.3:c.3503_3506del ENSP00000261917.3:p.Phe1168TrpfsTer12
NM_005477.2:c.3503_3506del NP_005468.1:p.Phe1168TrpfsTer12
XM_011521148.1:c.2285_2288del XP_011519450.1:p.Phe762TrpfsTer12
XM_011521148.2:c.2285_2288del XP_011519450.1:p.Phe762TrpfsTer12
NM_005477.3:c.3503_3506del MANE Select NP_005468.1:p.Phe1168TrpfsTer12