Canonical Allele Identifier: CA1543790313

Gene: HCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45645241G= , CM000667.2:g.45645241G=	GRCh38
NC_000005.9:g.45645343G= , CM000667.1:g.45645343G=	GRCh37
NC_000005.8:g.45681100G=	NCBI36
NG_042183.1:g.55878C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.793C= MANE Select	ENSP00000307342.4:p.Leu265=
ENST00000637256.1:n.21C=
ENST00000673735.1:c.793C=	ENSP00000501107.1:p.Leu265=
ENST00000303230.5:c.793C=	ENSP00000307342.4:p.Leu265=
ENST00000634658.1:c.793C=	ENSP00000489134.1:p.Leu265=
NM_021072.3:c.793C=	NP_066550.2:p.Leu265=
NM_021072.4:c.793C= MANE Select	NP_066550.2:p.Leu265=