Canonical Allele Identifier: CA2629389814
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367727del , CM000677.2:g.73367727del GRCh38
NC_000015.9:g.73660068del , CM000677.1:g.73660068del GRCh37
NC_000015.8:g.71447121del NCBI36
NG_009063.1:g.6540del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.546del MANE Select ENSP00000261917.3:p.Ser183ArgfsTer?
ENST00000261917.3:c.546del ENSP00000261917.3:p.Ser183ArgfsTer?
NM_005477.2:c.546del NP_005468.1:p.Ser183ArgfsTer?
NM_005477.3:c.546del MANE Select NP_005468.1:p.Ser183ArgfsTer?