Canonical Allele Identifier: CA393089398
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323880T>G , CM000677.2:g.73323880T>G GRCh38
NC_000015.9:g.73616221T>G , CM000677.1:g.73616221T>G GRCh37
NC_000015.8:g.71403274T>G NCBI36
NG_009063.1:g.50385A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2213A>C MANE Select ENSP00000261917.3:p.Glu738Ala
ENST00000261917.3:c.2213A>C ENSP00000261917.3:p.Glu738Ala
NM_005477.2:c.2213A>C NP_005468.1:p.Glu738Ala
XM_011521148.1:c.995A>C XP_011519450.1:p.Glu332Ala
XM_011521148.2:c.995A>C XP_011519450.1:p.Glu332Ala
NM_005477.3:c.2213A>C MANE Select NP_005468.1:p.Glu738Ala