Canonical Allele Identifier: CA1543790549

Gene: HCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45645383A= , CM000667.2:g.45645383A=	GRCh38
NC_000005.9:g.45645485A= , CM000667.1:g.45645485A=	GRCh37
NC_000005.8:g.45681242A=	NCBI36
NG_042183.1:g.55736T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000303230.6:c.651T= MANE Select	ENSP00000307342.4:p.Tyr217=
ENST00000673735.1:c.651T=	ENSP00000501107.1:p.Tyr217=
ENST00000303230.5:c.651T=	ENSP00000307342.4:p.Tyr217=
ENST00000634658.1:c.651T=	ENSP00000489134.1:p.Tyr217=
NM_021072.3:c.651T=	NP_066550.2:p.Tyr217=
NM_021072.4:c.651T= MANE Select	NP_066550.2:p.Tyr217=