Canonical Allele Identifier: CA1543790848

Gene: HCN1

Linked Data

• dbSNP Id: rs1745534157

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45645632_45645633insACAGTTTTCCTA , CM000667.2:g.45645632_45645633insACAGTTTTCCTA	GRCh38
NC_000005.9:g.45645734_45645735insACAGTTTTCCTA , CM000667.1:g.45645734_45645735insACAGTTTTCCTA	GRCh37
NC_000005.8:g.45681491_45681492insACAGTTTTCCTA	NCBI36
NG_042183.1:g.55486_55487insTAGGAAAACTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.426-25_426-24insTAGGAAAACTGT MANE Select	ENSP00000307342.4:n.426-25_426-24insTAGGAAAACTGT
ENST00000673735.1:c.426-25_426-24insTAGGAAAACTGT	ENSP00000501107.1:n.426-25_426-24insTAGGAAAACTGT
ENST00000303230.5:c.426-25_426-24insTAGGAAAACTGT	ENSP00000307342.4:n.426-25_426-24insTAGGAAAACTGT
ENST00000634658.1:c.426-25_426-24insTAGGAAAACTGT	ENSP00000489134.1:n.426-25_426-24insTAGGAAAACTGT
NM_021072.3:c.426-25_426-24insTAGGAAAACTGT	NP_066550.2:n.426-25_426-24insTAGGAAAACTGT
NM_021072.4:c.426-25_426-24insTAGGAAAACTGT MANE Select	NP_066550.2:n.426-25_426-24insTAGGAAAACTGT