Canonical Allele Identifier: CA2187169726

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73332145T= , CM000677.2:g.73332145T=	GRCh38
NC_000015.9:g.73624486T= , CM000677.1:g.73624486T=	GRCh37
NC_000015.8:g.71411539T=	NCBI36
NG_009063.1:g.42120A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.1357A= MANE Select	ENSP00000261917.3:p.Ile453=
ENST00000261917.3:c.1357A=	ENSP00000261917.3:p.Ile453=
NM_005477.2:c.1357A=	NP_005468.1:p.Ile453=
XM_011521148.1:c.139A=	XP_011519450.1:p.Ile47=
XM_011521148.2:c.139A=	XP_011519450.1:p.Ile47=
NM_005477.3:c.1357A= MANE Select	NP_005468.1:p.Ile453=