Canonical Allele Identifier: CA1543790191

Gene: HCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45645147C= , CM000667.2:g.45645147C=	GRCh38
NC_000005.9:g.45645249C= , CM000667.1:g.45645249C=	GRCh37
NC_000005.8:g.45681006C=	NCBI36
NG_042183.1:g.55972G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000303230.6:c.849+38G= MANE Select	ENSP00000307342.4:n.849+38G=
ENST00000637256.1:n.77+38G=
ENST00000673735.1:c.849+38G=	ENSP00000501107.1:n.849+38G=
ENST00000303230.5:c.849+38G=	ENSP00000307342.4:n.849+38G=
ENST00000634658.1:c.887G=	ENSP00000489134.1:p.Ter296=
NM_021072.3:c.849+38G=	NP_066550.2:n.849+38G=
NM_021072.4:c.849+38G= MANE Select	NP_066550.2:n.849+38G=