Canonical Allele Identifier: CA1543790133

Gene: HCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45645123T= , CM000667.2:g.45645123T=	GRCh38
NC_000005.9:g.45645225T= , CM000667.1:g.45645225T=	GRCh37
NC_000005.8:g.45680982T=	NCBI36
NG_042183.1:g.55996A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000303230.6:c.849+62A= MANE Select	ENSP00000307342.4:n.849+62A=
ENST00000637256.1:n.77+62A=
ENST00000673735.1:c.849+62A=	ENSP00000501107.1:n.849+62A=
ENST00000303230.5:c.849+62A=	ENSP00000307342.4:n.849+62A=
ENST00000634658.1:c.*23A=	ENSP00000489134.1:n.*23A=
NM_021072.3:c.849+62A=	NP_066550.2:n.849+62A=
NM_021072.4:c.849+62A= MANE Select	NP_066550.2:n.849+62A=