Canonical Allele Identifier: CA1543790757

Gene: HCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45645546C= , CM000667.2:g.45645546C=	GRCh38
NC_000005.9:g.45645648C= , CM000667.1:g.45645648C=	GRCh37
NC_000005.8:g.45681405C=	NCBI36
NG_042183.1:g.55573G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.488G= MANE Select	ENSP00000307342.4:p.Gly163=
ENST00000673735.1:c.488G=	ENSP00000501107.1:p.Gly163=
ENST00000303230.5:c.488G=	ENSP00000307342.4:p.Gly163=
ENST00000634658.1:c.488G=	ENSP00000489134.1:p.Gly163=
NM_021072.3:c.488G=	NP_066550.2:p.Gly163=
NM_021072.4:c.488G= MANE Select	NP_066550.2:p.Gly163=