Canonical Allele Identifier: CA2187167439

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73329617G= , CM000677.2:g.73329617G=	GRCh38
NC_000015.9:g.73621958G= , CM000677.1:g.73621958G=	GRCh37
NC_000015.8:g.71409011G=	NCBI36
NG_009063.1:g.44648C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1546C= MANE Select	ENSP00000261917.3:p.Leu516=
ENST00000261917.3:c.1546C=	ENSP00000261917.3:p.Leu516=
NM_005477.2:c.1546C=	NP_005468.1:p.Leu516=
XM_011521148.1:c.328C=	XP_011519450.1:p.Leu110=
XM_011521148.2:c.328C=	XP_011519450.1:p.Leu110=
NM_005477.3:c.1546C= MANE Select	NP_005468.1:p.Leu516=