Canonical Allele Identifier: CA917464373

Gene: HCN1

Linked Data

• dbSNP Id: rs1561164193

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45462244_45462247dup , CM000667.2:g.45462244_45462247dup	GRCh38
NC_000005.9:g.45462346_45462349dup , CM000667.1:g.45462346_45462349dup	GRCh37
NC_000005.8:g.45498103_45498106dup	NCBI36
NG_042183.1:g.238875_238878dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.850-237_850-234dup MANE Select	ENSP00000307342.4:n.850-237_850-234dup
ENST00000637305.1:n.13-237_13-234dup
ENST00000673735.1:c.850-237_850-234dup	ENSP00000501107.1:n.850-237_850-234dup
ENST00000303230.5:c.850-237_850-234dup	ENSP00000307342.4:n.850-237_850-234dup
NM_021072.3:c.850-237_850-234dup	NP_066550.2:n.850-237_850-234dup
NM_021072.4:c.850-237_850-234dup MANE Select	NP_066550.2:n.850-237_850-234dup