Canonical Allele Identifier: CA2187186326
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322629_73322631delinsTTC , CM000677.2:g.73322629_73322631delinsTTC GRCh38
NC_000015.9:g.73614970_73614972delinsTTC , CM000677.1:g.73614970_73614972delinsTTC GRCh37
NC_000015.8:g.71402023_71402025delinsTTC NCBI36
NG_009063.1:g.51634_51636delinsGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3462_3464delinsGAA MANE Select ENSP00000261917.3:p.Arg1154=
ENST00000261917.3:c.3462_3464delinsGAA ENSP00000261917.3:p.Arg1154=
NM_005477.2:c.3462_3464delinsGAA NP_005468.1:p.Arg1154=
XM_011521148.1:c.2244_2246delinsGAA XP_011519450.1:p.Arg748=
XM_011521148.2:c.2244_2246delinsGAA XP_011519450.1:p.Arg748=
NM_005477.3:c.3462_3464delinsGAA MANE Select NP_005468.1:p.Arg1154=
Search 100 bp 5'
Search 100 bp 3'