Canonical Allele Identifier: CA2840286486
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323575del , CM000677.2:g.73323575del GRCh38
NC_000015.9:g.73615916del , CM000677.1:g.73615916del GRCh37
NC_000015.8:g.71402969del NCBI36
NG_009063.1:g.50690del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2518del MANE Select ENSP00000261917.3:p.Ala840ProfsTer?
ENST00000261917.3:c.2518del ENSP00000261917.3:p.Ala840ProfsTer?
NM_005477.2:c.2518del NP_005468.1:p.Ala840ProfsTer?
XM_011521148.1:c.1300del XP_011519450.1:p.Ala434ProfsTer?
XM_011521148.2:c.1300del XP_011519450.1:p.Ala434ProfsTer?
NM_005477.3:c.2518del MANE Select NP_005468.1:p.Ala840ProfsTer?