Canonical Allele Identifier: CA2629389854
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367949del , CM000677.2:g.73367949del GRCh38
NC_000015.9:g.73660290del , CM000677.1:g.73660290del GRCh37
NC_000015.8:g.71447343del NCBI36
NG_009063.1:g.6317del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.323del MANE Select ENSP00000261917.3:p.Gly108AlafsTer?
ENST00000261917.3:c.323del ENSP00000261917.3:p.Gly108AlafsTer?
NM_005477.2:c.323del NP_005468.1:p.Gly108AlafsTer?
NM_005477.3:c.323del MANE Select NP_005468.1:p.Gly108AlafsTer?