Canonical Allele Identifier: CA1543688727

Gene: HCN1

Linked Data

• dbSNP Id: rs1741177271

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45462255_45462258del , CM000667.2:g.45462255_45462258del	GRCh38
NC_000005.9:g.45462357_45462360del , CM000667.1:g.45462357_45462360del	GRCh37
NC_000005.8:g.45498114_45498117del	NCBI36
NG_042183.1:g.238867_238870del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.850-245_850-242del MANE Select	ENSP00000307342.4:n.850-245_850-242del
ENST00000637305.1:n.13-245_13-242del
ENST00000673735.1:c.850-245_850-242del	ENSP00000501107.1:n.850-245_850-242del
ENST00000303230.5:c.850-245_850-242del	ENSP00000307342.4:n.850-245_850-242del
NM_021072.3:c.850-245_850-242del	NP_066550.2:n.850-245_850-242del
NM_021072.4:c.850-245_850-242del MANE Select	NP_066550.2:n.850-245_850-242del