Canonical Allele Identifier: CA2187188557

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323598A= , CM000677.2:g.73323598A=	GRCh38
NC_000015.9:g.73615939A= , CM000677.1:g.73615939A=	GRCh37
NC_000015.8:g.71402992A=	NCBI36
NG_009063.1:g.50667T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.2495T= MANE Select	ENSP00000261917.3:p.Leu832=
ENST00000261917.3:c.2495T=	ENSP00000261917.3:p.Leu832=
NM_005477.2:c.2495T=	NP_005468.1:p.Leu832=
XM_011521148.1:c.1277T=	XP_011519450.1:p.Leu426=
XM_011521148.2:c.1277T=	XP_011519450.1:p.Leu426=
NM_005477.3:c.2495T= MANE Select	NP_005468.1:p.Leu832=