Canonical Allele Identifier: CA2187186985

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322915G= , CM000677.2:g.73322915G=	GRCh38
NC_000015.9:g.73615256G= , CM000677.1:g.73615256G=	GRCh37
NC_000015.8:g.71402309G=	NCBI36
NG_009063.1:g.51350C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3178C= MANE Select	ENSP00000261917.3:p.Pro1060=
ENST00000261917.3:c.3178C=	ENSP00000261917.3:p.Pro1060=
NM_005477.2:c.3178C=	NP_005468.1:p.Pro1060=
XM_011521148.1:c.1960C=	XP_011519450.1:p.Pro654=
XM_011521148.2:c.1960C=	XP_011519450.1:p.Pro654=
NM_005477.3:c.3178C= MANE Select	NP_005468.1:p.Pro1060=