Canonical Allele Identifier: CA2187186298
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322588_73322594delinsCAAACAA , CM000677.2:g.73322588_73322594delinsCAAACAA GRCh38
NC_000015.9:g.73614929_73614935delinsCAAACAA , CM000677.1:g.73614929_73614935delinsCAAACAA GRCh37
NC_000015.8:g.71401982_71401988delinsCAAACAA NCBI36
NG_009063.1:g.51671_51677delinsTTGTTTG

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3499_3505delinsTTGTTTG MANE Select ENSP00000261917.3:p.Leu1167=
ENST00000261917.3:c.3499_3505delinsTTGTTTG ENSP00000261917.3:p.Leu1167=
NM_005477.2:c.3499_3505delinsTTGTTTG NP_005468.1:p.Leu1167=
XM_011521148.1:c.2281_2287delinsTTGTTTG XP_011519450.1:p.Leu761=
XM_011521148.2:c.2281_2287delinsTTGTTTG XP_011519450.1:p.Leu761=
NM_005477.3:c.3499_3505delinsTTGTTTG MANE Select NP_005468.1:p.Leu1167=