Canonical Allele Identifier: CA2629389824
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367857_73367858insC , CM000677.2:g.73367857_73367858insC GRCh38
NC_000015.9:g.73660198_73660199insC , CM000677.1:g.73660198_73660199insC GRCh37
NC_000015.8:g.71447251_71447252insC NCBI36
NG_009063.1:g.6407_6408insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.413_414insG MANE Select ENSP00000261917.3:p.Gly140ArgfsTer?
ENST00000261917.3:c.413_414insG ENSP00000261917.3:p.Gly140ArgfsTer?
NM_005477.2:c.413_414insG NP_005468.1:p.Gly140ArgfsTer?
NM_005477.3:c.413_414insG MANE Select NP_005468.1:p.Gly140ArgfsTer?