Canonical Allele Identifier: CA2804726809

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322593_73322594insCACCC , CM000677.2:g.73322593_73322594insCACCC	GRCh38
NC_000015.9:g.73614934_73614935insCACCC , CM000677.1:g.73614934_73614935insCACCC	GRCh37
NC_000015.8:g.71401987_71401988insCACCC	NCBI36
NG_009063.1:g.51671_51672insGGGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3499_3500insGGGTG MANE Select	ENSP00000261917.3:p.Leu1167TrpfsTer16
ENST00000261917.3:c.3499_3500insGGGTG	ENSP00000261917.3:p.Leu1167TrpfsTer16
NM_005477.2:c.3499_3500insGGGTG	NP_005468.1:p.Leu1167TrpfsTer16
XM_011521148.1:c.2281_2282insGGGTG	XP_011519450.1:p.Leu761TrpfsTer16
XM_011521148.2:c.2281_2282insGGGTG	XP_011519450.1:p.Leu761TrpfsTer16
NM_005477.3:c.3499_3500insGGGTG MANE Select	NP_005468.1:p.Leu1167TrpfsTer16