Canonical Allele Identifier: CA2841139552
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329766del , CM000677.2:g.73329766del GRCh38
NC_000015.9:g.73622107del , CM000677.1:g.73622107del GRCh37
NC_000015.8:g.71409160del NCBI36
NG_009063.1:g.44500del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1398del MANE Select ENSP00000261917.3:p.Tyr467ThrfsTer7
ENST00000261917.3:c.1398del ENSP00000261917.3:p.Tyr467ThrfsTer7
NM_005477.2:c.1398del NP_005468.1:p.Tyr467ThrfsTer7
XM_011521148.1:c.180del XP_011519450.1:p.Tyr61ThrfsTer7
XM_011521148.2:c.180del XP_011519450.1:p.Tyr61ThrfsTer7
NM_005477.3:c.1398del MANE Select NP_005468.1:p.Tyr467ThrfsTer7