Canonical Allele Identifier: CA1543688395

Gene: HCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45461970A= , CM000667.2:g.45461970A=	GRCh38
NC_000005.9:g.45462072A= , CM000667.1:g.45462072A=	GRCh37
NC_000005.8:g.45497829A=	NCBI36
NG_042183.1:g.239149T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.887T= MANE Select	ENSP00000307342.4:p.Val296=
ENST00000637305.1:n.50T=
ENST00000673735.1:c.887T=	ENSP00000501107.1:p.Val296=
ENST00000303230.5:c.887T=	ENSP00000307342.4:p.Val296=
NM_021072.3:c.887T=	NP_066550.2:p.Val296=
NM_021072.4:c.887T= MANE Select	NP_066550.2:p.Val296=