Canonical Allele Identifier: CA393093326
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329576T>A , CM000677.2:g.73329576T>A GRCh38
NC_000015.9:g.73621917T>A , CM000677.1:g.73621917T>A GRCh37
NC_000015.8:g.71408970T>A NCBI36
NG_009063.1:g.44689A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1587A>T MANE Select ENSP00000261917.3:p.Glu529Asp
ENST00000261917.3:c.1587A>T ENSP00000261917.3:p.Glu529Asp
NM_005477.2:c.1587A>T NP_005468.1:p.Glu529Asp
XM_011521148.1:c.369A>T XP_011519450.1:p.Glu123Asp
XM_011521148.2:c.369A>T XP_011519450.1:p.Glu123Asp
NM_005477.3:c.1587A>T MANE Select NP_005468.1:p.Glu529Asp