Canonical Allele Identifier: CA2187188106

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323358T= , CM000677.2:g.73323358T=	GRCh38
NC_000015.9:g.73615699T= , CM000677.1:g.73615699T=	GRCh37
NC_000015.8:g.71402752T=	NCBI36
NG_009063.1:g.50907A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.2735A= MANE Select	ENSP00000261917.3:p.Lys912=
ENST00000261917.3:c.2735A=	ENSP00000261917.3:p.Lys912=
NM_005477.2:c.2735A=	NP_005468.1:p.Lys912=
XM_011521148.1:c.1517A=	XP_011519450.1:p.Lys506=
XM_011521148.2:c.1517A=	XP_011519450.1:p.Lys506=
NM_005477.3:c.2735A= MANE Select	NP_005468.1:p.Lys912=