Canonical Allele Identifier: CA2629370545
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323068del , CM000677.2:g.73323068del GRCh38
NC_000015.9:g.73615409del , CM000677.1:g.73615409del GRCh37
NC_000015.8:g.71402462del NCBI36
NG_009063.1:g.51200del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3028del MANE Select ENSP00000261917.3:p.Ala1010ProfsTer8
ENST00000261917.3:c.3028del ENSP00000261917.3:p.Ala1010ProfsTer8
NM_005477.2:c.3028del NP_005468.1:p.Ala1010ProfsTer8
XM_011521148.1:c.1810del XP_011519450.1:p.Ala604ProfsTer8
XM_011521148.2:c.1810del XP_011519450.1:p.Ala604ProfsTer8
NM_005477.3:c.3028del MANE Select NP_005468.1:p.Ala1010ProfsTer8