Canonical Allele Identifier: CA1543688643

Gene: HCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45462136_45462137delinsAG , CM000667.2:g.45462136_45462137delinsAG	GRCh38
NC_000005.9:g.45462238_45462239delinsAG , CM000667.1:g.45462238_45462239delinsAG	GRCh37
NC_000005.8:g.45497995_45497996delinsAG	NCBI36
NG_042183.1:g.238982_238983delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.850-130_850-129delinsCT MANE Select	ENSP00000307342.4:n.850-130_850-129delinsCT
ENST00000637305.1:n.13-130_13-129delinsCT
ENST00000673735.1:c.850-130_850-129delinsCT	ENSP00000501107.1:n.850-130_850-129delinsCT
ENST00000303230.5:c.850-130_850-129delinsCT	ENSP00000307342.4:n.850-130_850-129delinsCT
NM_021072.3:c.850-130_850-129delinsCT	NP_066550.2:n.850-130_850-129delinsCT
NM_021072.4:c.850-130_850-129delinsCT MANE Select	NP_066550.2:n.850-130_850-129delinsCT