Canonical Allele Identifier: CA393085059
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322584G>T , CM000677.2:g.73322584G>T GRCh38
NC_000015.9:g.73614925G>T , CM000677.1:g.73614925G>T GRCh37
NC_000015.8:g.71401978G>T NCBI36
NG_009063.1:g.51681C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3509C>A MANE Select ENSP00000261917.3:p.Ala1170Glu
ENST00000261917.3:c.3509C>A ENSP00000261917.3:p.Ala1170Glu
NM_005477.2:c.3509C>A NP_005468.1:p.Ala1170Glu
XM_011521148.1:c.2291C>A XP_011519450.1:p.Ala764Glu
XM_011521148.2:c.2291C>A XP_011519450.1:p.Ala764Glu
NM_005477.3:c.3509C>A MANE Select NP_005468.1:p.Ala1170Glu