Canonical Allele Identifier: CA393086573
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323108C>A , CM000677.2:g.73323108C>A GRCh38
NC_000015.9:g.73615449C>A , CM000677.1:g.73615449C>A GRCh37
NC_000015.8:g.71402502C>A NCBI36
NG_009063.1:g.51157G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2985G>T MANE Select ENSP00000261917.3:p.Glu995Asp
ENST00000261917.3:c.2985G>T ENSP00000261917.3:p.Glu995Asp
NM_005477.2:c.2985G>T NP_005468.1:p.Glu995Asp
XM_011521148.1:c.1767G>T XP_011519450.1:p.Glu589Asp
XM_011521148.2:c.1767G>T XP_011519450.1:p.Glu589Asp
NM_005477.3:c.2985G>T MANE Select NP_005468.1:p.Glu995Asp