Canonical Allele Identifier: CA1543688341

Gene: HCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45461944T= , CM000667.2:g.45461944T=	GRCh38
NC_000005.9:g.45462046T= , CM000667.1:g.45462046T=	GRCh37
NC_000005.8:g.45497803T=	NCBI36
NG_042183.1:g.239175A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.913A= MANE Select	ENSP00000307342.4:p.Met305=
ENST00000637305.1:n.76A=
ENST00000673735.1:c.913A=	ENSP00000501107.1:p.Met305=
ENST00000303230.5:c.913A=	ENSP00000307342.4:p.Met305=
NM_021072.3:c.913A=	NP_066550.2:p.Met305=
NM_021072.4:c.913A= MANE Select	NP_066550.2:p.Met305=