Canonical Allele Identifier: CA2187187341

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323051A= , CM000677.2:g.73323051A=	GRCh38
NC_000015.9:g.73615392A= , CM000677.1:g.73615392A=	GRCh37
NC_000015.8:g.71402445A=	NCBI36
NG_009063.1:g.51214T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3042T= MANE Select	ENSP00000261917.3:p.Ala1014=
ENST00000261917.3:c.3042T=	ENSP00000261917.3:p.Ala1014=
NM_005477.2:c.3042T=	NP_005468.1:p.Ala1014=
XM_011521148.1:c.1824T=	XP_011519450.1:p.Ala608=
XM_011521148.2:c.1824T=	XP_011519450.1:p.Ala608=
NM_005477.3:c.3042T= MANE Select	NP_005468.1:p.Ala1014=