Canonical Allele Identifier: CA2187186522

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322706_73322715delinsACTGCCCCCG , CM000677.2:g.73322706_73322715delinsACTGCCCCCG	GRCh38
NC_000015.9:g.73615047_73615056delinsACTGCCCCCG , CM000677.1:g.73615047_73615056delinsACTGCCCCCG	GRCh37
NC_000015.8:g.71402100_71402109delinsACTGCCCCCG	NCBI36
NG_009063.1:g.51550_51559delinsCGGGGGCAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3378_3387delinsCGGGGGCAGT MANE Select	ENSP00000261917.3:p.Ser1126=
ENST00000261917.3:c.3378_3387delinsCGGGGGCAGT	ENSP00000261917.3:p.Ser1126=
NM_005477.2:c.3378_3387delinsCGGGGGCAGT	NP_005468.1:p.Ser1126=
XM_011521148.1:c.2160_2169delinsCGGGGGCAGT	XP_011519450.1:p.Ser720=
XM_011521148.2:c.2160_2169delinsCGGGGGCAGT	XP_011519450.1:p.Ser720=
NM_005477.3:c.3378_3387delinsCGGGGGCAGT MANE Select	NP_005468.1:p.Ser1126=