Canonical Allele Identifier: CA2187186999

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322922T= , CM000677.2:g.73322922T=	GRCh38
NC_000015.9:g.73615263T= , CM000677.1:g.73615263T=	GRCh37
NC_000015.8:g.71402316T=	NCBI36
NG_009063.1:g.51343A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3171A= MANE Select	ENSP00000261917.3:p.Ala1057=
ENST00000261917.3:c.3171A=	ENSP00000261917.3:p.Ala1057=
NM_005477.2:c.3171A=	NP_005468.1:p.Ala1057=
XM_011521148.1:c.1953A=	XP_011519450.1:p.Ala651=
XM_011521148.2:c.1953A=	XP_011519450.1:p.Ala651=
NM_005477.3:c.3171A= MANE Select	NP_005468.1:p.Ala1057=