Canonical Allele Identifier: CA1543688656

Gene: HCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45462155_45462159delinsATTTC , CM000667.2:g.45462155_45462159delinsATTTC	GRCh38
NC_000005.9:g.45462257_45462261delinsATTTC , CM000667.1:g.45462257_45462261delinsATTTC	GRCh37
NC_000005.8:g.45498014_45498018delinsATTTC	NCBI36
NG_042183.1:g.238960_238964delinsGAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.850-152_850-148delinsGAAAT MANE Select	ENSP00000307342.4:n.850-152_850-148delinsGAAAT
ENST00000637305.1:n.13-152_13-148delinsGAAAT
ENST00000673735.1:c.850-152_850-148delinsGAAAT	ENSP00000501107.1:n.850-152_850-148delinsGAAAT
ENST00000303230.5:c.850-152_850-148delinsGAAAT	ENSP00000307342.4:n.850-152_850-148delinsGAAAT
NM_021072.3:c.850-152_850-148delinsGAAAT	NP_066550.2:n.850-152_850-148delinsGAAAT
NM_021072.4:c.850-152_850-148delinsGAAAT MANE Select	NP_066550.2:n.850-152_850-148delinsGAAAT