Canonical Allele Identifier: CA2187186974

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322911G= , CM000677.2:g.73322911G=	GRCh38
NC_000015.9:g.73615252G= , CM000677.1:g.73615252G=	GRCh37
NC_000015.8:g.71402305G=	NCBI36
NG_009063.1:g.51354C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3182C= MANE Select	ENSP00000261917.3:p.Pro1061=
ENST00000261917.3:c.3182C=	ENSP00000261917.3:p.Pro1061=
NM_005477.2:c.3182C=	NP_005468.1:p.Pro1061=
XM_011521148.1:c.1964C=	XP_011519450.1:p.Pro655=
XM_011521148.2:c.1964C=	XP_011519450.1:p.Pro655=
NM_005477.3:c.3182C= MANE Select	NP_005468.1:p.Pro1061=