Canonical Allele Identifier: CA2187169765

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73332171T= , CM000677.2:g.73332171T=	GRCh38
NC_000015.9:g.73624512T= , CM000677.1:g.73624512T=	GRCh37
NC_000015.8:g.71411565T=	NCBI36
NG_009063.1:g.42094A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.1331A= MANE Select	ENSP00000261917.3:p.Asp444=
ENST00000261917.3:c.1331A=	ENSP00000261917.3:p.Asp444=
NM_005477.2:c.1331A=	NP_005468.1:p.Asp444=
XM_011521148.1:c.113A=	XP_011519450.1:p.Asp38=
XM_011521148.2:c.113A=	XP_011519450.1:p.Asp38=
NM_005477.3:c.1331A= MANE Select	NP_005468.1:p.Asp444=