Canonical Allele Identifier: CA444401453

Gene: HCN1

Linked Data

• MyVariant Identifiers: chr5:g.45645635A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45645533A>G , CM000667.2:g.45645533A>G	GRCh38
NC_000005.9:g.45645635A>G , CM000667.1:g.45645635A>G	GRCh37
NC_000005.8:g.45681392A>G	NCBI36
NG_042183.1:g.55586T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.501T>C MANE Select	ENSP00000307342.4:p.Phe167=
ENST00000673735.1:c.501T>C	ENSP00000501107.1:p.Phe167=
ENST00000303230.5:c.501T>C	ENSP00000307342.4:p.Phe167=
ENST00000634658.1:c.501T>C	ENSP00000489134.1:p.Phe167=
NM_021072.3:c.501T>C	NP_066550.2:p.Phe167=
NM_021072.4:c.501T>C MANE Select	NP_066550.2:p.Phe167=