Canonical Allele Identifier: CA2187186325

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322628C= , CM000677.2:g.73322628C=	GRCh38
NC_000015.9:g.73614969C= , CM000677.1:g.73614969C=	GRCh37
NC_000015.8:g.71402022C=	NCBI36
NG_009063.1:g.51637G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3465G= MANE Select	ENSP00000261917.3:p.Lys1155=
ENST00000261917.3:c.3465G=	ENSP00000261917.3:p.Lys1155=
NM_005477.2:c.3465G=	NP_005468.1:p.Lys1155=
XM_011521148.1:c.2247G=	XP_011519450.1:p.Lys749=
XM_011521148.2:c.2247G=	XP_011519450.1:p.Lys749=
NM_005477.3:c.3465G= MANE Select	NP_005468.1:p.Lys1155=